ID: 127886143 | H3K4me1 hESC enhancer GRCh37_chr17:19294419-19295332 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19391106..19392019) | | |
ID: 127886142 | H3K4me1 hESC enhancer GRCh37_chr17:19289883-19290428 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19386570..19387115) | | |
ID: 127886141 | H3K4me1 hESC enhancer GRCh37_chr17:19289337-19289882 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19386024..19386569) | | |
ID: 127886140 | H3K4me1 hESC enhancer GRCh37_chr17:19288791-19289336 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19385478..19386023) | | |
ID: 127886139 | H3K4me1 hESC enhancer GRCh37_chr17:19286483-19286983 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19383170..19383670) | | |
ID: 127886138 | H3K4me1 hESC enhancer GRCh37_chr17:19285982-19286482 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19382669..19383169) | | |
ID: 127886137 | H3K4me1 hESC enhancer GRCh37_chr17:19283774-19284736 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19380461..19381423) | | |
ID: 127886136 | H3K4me1 hESC enhancer GRCh37_chr17:19275949-19276498 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19372636..19373185) | | |
ID: 127886135 | H3K4me1 hESC enhancer GRCh37_chr17:19266095-19266879 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19362782..19363566) | | |
ID: 127886134 | H3K4me1 hESC enhancer GRCh37_chr17:19261015-19261514 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19357702..19358201) | | |
ID: 127886133 | H3K4me1 hESC enhancer GRCh37_chr17:19244665-19245232 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19341352..19341919) | | |
ID: 127886132 | H3K4me1 hESC enhancer GRCh37_chr17:19237143-19237914 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19333830..19334601) | | |
ID: 127886131 | H3K4me1 hESC enhancer GRCh37_chr17:19234824-19235596 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19331511..19332283) | | |
ID: 127886130 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:19220479-19221018 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19317166..19317705) | | |
ID: 127886129 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:19213152-19214067 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19309839..19310754) | | |
ID: 127886128 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:19212235-19213151 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19308922..19309838) | | |
ID: 127886127 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:19192933-19193526 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19289620..19290213) | | |
ID: 121852925 | Sharpr-MPRA regulatory region 2588 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19345596..19345890) | | |
ID: 105371573 | uncharacterized LOC105371573 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19362777..19371732) | | |
ID: 100874018 | EPN2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (19296596..19306261, complement) | | |