| ID: 127270503 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:156149713-156150215 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156179922..156180424) | | |
| ID: 127270502 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:156146693-156147195 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156176902..156177404) | | |
| ID: 127270501 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:156096352-156097337 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156126561..156127546) | | |
| ID: 127270500 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:156093390-156094377 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156123599..156124586) | | |
| ID: 127270499 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:156090429-156091415 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156120638..156121624) | | |
| ID: 127270498 | H3K4me1 hESC enhancer GRCh37_chr1:156087275-156087774 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156117484..156117983) | | |
| ID: 127270497 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:156077037-156077778 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156107246..156107987) | | |
| ID: 127270496 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:156067261-156068134 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156097470..156098343) | | |
| ID: 127270495 | H3K27ac hESC enhancer GRCh37_chr1:156056191-156057025 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156086400..156087234) | | |
| ID: 127270494 | H3K27ac hESC enhancer GRCh37_chr1:156052057-156052870 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156082266..156083079) | | |
| ID: 127270493 | H3K27ac hESC enhancer GRCh37_chr1:156051244-156052056 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156081453..156082265) | | |
| ID: 126805877 | MED14-independent group 3 enhancer GRCh37_chr1:156099693-156100892 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156129902..156131101) | | |
| ID: 122128444 | H3K27ac-H3K4me1 hESC enhancers GRCh37_chr1:156045982-156046889 and GRCh37_chr1:156046890-156047796 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156076191..156078005) | | |
| ID: 121725059 | Sharpr-MPRA regulatory region 15377 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156090718..156091012) | | |
| ID: 120893162 | Sharpr-MPRA regulatory region 4592 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156125128..156125432) | | |
| ID: 110121262 | VISTA enhancer hs2129 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156102512..156107245) | | |
| ID: 92312 | mex-3 RNA binding family member A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156072013..156082465, complement) | MEX-3A, RKHD4, RNF162 | 611007 |
| ID: 64218 | semaphorin 4A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156147373..156177744) | CORD10, RP35, SEMAB, SEMB | 607292 |
| ID: 4000 | lamin A/C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156082573..156140081) | CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1 | 150330 |