| ID: 127273363 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:51254469-51255168 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (51027331..51028030) | | |
| ID: 127273362 | OCT4-NANOG hESC enhancer GRCh37_chr2:51240083-51240639 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (51012945..51013501) | | |
| ID: 127273361 | OCT4-NANOG hESC enhancer GRCh37_chr2:51227905-51228438 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (51000767..51001300) | | |
| ID: 127273360 | H3K4me1 hESC enhancer GRCh37_chr2:50573861-50574798 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50346723..50347660) | | |
| ID: 127273359 | H3K4me1 hESC enhancer GRCh37_chr2:50572921-50573860 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50345783..50346722) | | |
| ID: 127273358 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:50311785-50312297 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50084647..50085159) | | |
| ID: 127273357 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:50311271-50311784 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50084133..50084646) | | |
| ID: 127273356 | OCT4-NANOG hESC enhancer GRCh37_chr2:50231574-50232307 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50004436..50005169) | | |
| ID: 127273355 | OCT4-NANOG hESC enhancer GRCh37_chr2:50163910-50164578 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (49936772..49937440) | | |
| ID: 127273354 | H3K4me1 hESC enhancer GRCh37_chr2:49999711-50000210 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (49772573..49773072) | | |
| ID: 126806216 | MED14-independent group 3 enhancer GRCh37_chr2:51483602-51484801 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (51256464..51257663) | | |
| ID: 124906006 | uncharacterized LOC124906006 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50814164..50820728) | | |
| ID: 114827832 | VISTA enhancer hs2343 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (49971632..49975473) | | |
| ID: 110121071 | VISTA enhancer hs1348 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50613290..50616899) | | |
| ID: 107075283 | MT-CO1 pseudogene 42 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50588690..50589415, complement) | | |
| ID: 105377627 | uncharacterized LOC105377627 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (51330841..51350197, complement) | | |
| ID: 103504737 | microRNA 8485 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50696172..50696262, complement) | hsa-mir-8485 | |
| ID: 101927089 | uncharacterized LOC101927089 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (50620924..50632732) | | |
| ID: 730100 | NRXN1 divergent transcript [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (51032601..52407917) | | |
| ID: 130728 | ribosomal protein L7 pseudogene 13 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (49878612..49879434) | RPL7_4_218 | |