ID: 127883590 | H3K4me1 hESC enhancer GRCh37_chr16:29260095-29260595 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29248774..29249274) | | |
ID: 127883589 | H3K27ac hESC enhancer GRCh37_chr16:29233140-29233640 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29221819..29222319) | | |
ID: 127883588 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:29232263-29232832 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29220942..29221511) | | |
ID: 127883587 | H3K4me1 hESC enhancer GRCh37_chr16:29209784-29210284 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29198463..29198963) | | |
ID: 127883586 | H3K4me1 hESC enhancer GRCh37_chr16:29203636-29204362 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29192315..29193041) | | |
ID: 127883585 | H3K4me1 hESC enhancer GRCh37_chr16:29177699-29178199 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29166378..29166878) | | |
ID: 127883584 | H3K4me1 hESC enhancer GRCh37_chr16:29163489-29164159 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29152168..29152838) | | |
ID: 127883583 | H3K4me1 hESC enhancer GRCh37_chr16:29155769-29156455 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29144448..29145134) | | |
ID: 127883582 | H3K4me1 hESC enhancer GRCh37_chr16:29155082-29155768 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29143761..29144447) | | |
ID: 127883581 | H3K4me1 hESC enhancer GRCh37_chr16:29145325-29145825 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29134004..29134504) | | |
ID: 127883580 | H3K4me1 hESC enhancer GRCh37_chr16:29141163-29141951 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29129842..29130630) | | |
ID: 127883579 | H3K4me1 hESC enhancer GRCh37_chr16:29126448-29126996 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29115127..29115675) | | |
ID: 126862328 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr16:29196056-29197255 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29184735..29185934) | | |
ID: 126862327 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr16:29166386-29167585 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29155065..29156264) | | |
ID: 125146438 | Sharpr-MPRA regulatory region 8859 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29202608..29202902) | | |
ID: 125146437 | Sharpr-MPRA regulatory region 414 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29156588..29156882) | | |
ID: 124903676 | uncharacterized LOC124903676 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29256044..29258779, complement) | | |
ID: 124903671 | uncharacterized LOC124903671 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29127070..29132656, complement) | | |
ID: 108281183 | RRN3P2-SNX29P2 intergenic nontranscribed DNase I hypersensitive site-defined enhancer [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29186703..29187297) | | |
ID: 102723708 | uncharacterized LOC102723708 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29225583..29228523, complement) | | |