ID: 127459529 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:54934747-54935540 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (54022187..54022980) | | |
ID: 127459528 | H3K4me1 hESC enhancer GRCh37_chr8:54793963-54794594 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53881403..53882034) | | |
ID: 127459527 | H3K4me1 hESC enhancer GRCh37_chr8:54793331-54793962 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53880712..53881402) | | |
ID: 127459526 | H3K4me1 hESC enhancer GRCh37_chr8:54789287-54789787 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53876727..53877227) | | |
ID: 126860390 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:54640179-54641378 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53727619..53728818) | | |
ID: 113788287 | Sharpr-MPRA regulatory region 5984 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53879829..53880123) | | |
ID: 111811969 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:54856969-54858168 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53944409..53945608) | | |
ID: 106480147 | RNA, U6 small nuclear 1331, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53914719..53914824) | | |
ID: 100131254 | ESF1, nucleolar pre-rRNA processing protein, homolog (S. cerevisiae) pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53971598..53973892) | | |
ID: 100130300 | RPS27A pseudogene 13 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53887008..53887479, complement) | RPS27A_4_904 | |
ID: 100129667 | chromosome 5 open reading frame 13 pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53712697..53712896) | | |
ID: 51606 | ATPase H+ transporting V1 subunit H [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53715543..53843245, complement) | CGI-11, MSTP042, NBP1, SFD, SFDalpha, SFDbeta, VMA13 | 608861 |
ID: 8601 | regulator of G protein signaling 20 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53851795..53959303) | RGSZ1, ZGAP1, g(z)GAP, gz-GAP | 607193 |
ID: 6917 | transcription elongation factor A1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53966556..54022448, complement) | GTF2S, SII, TCEA, TF2S, TFIIS | 601425 |