ID: 127888043 | H3K4me1 hESC enhancer GRCh37_chr17:74723821-74724449 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76727739..76728367) | | |
ID: 127888042 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:74722561-74723190 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76726479..76727219) | | |
ID: 127888041 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:74697733-74698236 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76701651..76702154) | | |
ID: 127888040 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:74696723-74697227 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76700641..76701145) | | |
ID: 127888039 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:74696218-74696722 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76700136..76700640) | | |
ID: 127888038 | H3K4me1 hESC enhancer GRCh37_chr17:74694343-74694895 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76698261..76698813) | | |
ID: 127888037 | H3K4me1 hESC enhancer GRCh37_chr17:74693789-74694342 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76697707..76698260) | | |
ID: 127888036 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:74693235-74693788 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76697153..76697706) | | |
ID: 127888035 | H3K4me1 hESC enhancer GRCh37_chr17:74682678-74683473 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76686596..76687391) | | |
ID: 127888034 | H3K4me1 hESC enhancer GRCh37_chr17:74680151-74680695 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76684069..76684613) | | |
ID: 127888033 | H3K4me1 hESC enhancer GRCh37_chr17:74678511-74679057 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76682429..76682975) | | |
ID: 127888032 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:74666855-74667812 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76670773..76671759) | | |
ID: 106481883 | RNA, U6 small nuclear 227, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76656316..76656418) | | |
ID: 106480313 | RNY4 pseudogene 36 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76703632..76703727, complement) | | |
ID: 105274304 | uncharacterized LOC105274304 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76671928..76673658) | | |
ID: 439921 | matrix remodeling associated 7 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76672551..76710965, complement) | | |
ID: 124512 | methyltransferase 23, arginine [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76726041..76733881) | C17orf95, MRT44 | 615262 |
ID: 23210 | jumonji domain containing 6, arginine demethylase and lysine hydroxylase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76712836..76726606, complement) | PSR, PTDSR, PTDSR1 | 604914 |