ID: 127882737 | H3K27ac hESC enhancer GRCh37_chr16:1662757-1663257 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1612717..1613256) | | |
ID: 127882736 | H3K27ac hESC enhancer GRCh37_chr16:1662256-1662756 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1612017..1612755) | | |
ID: 127882735 | H3K4me1 hESC enhancer GRCh37_chr16:1611806-1612415 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1561805..1562414) | | |
ID: 127882734 | H3K4me1 hESC enhancer GRCh37_chr16:1605115-1605614 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1555114..1555613) | | |
ID: 127882733 | H3K4me1 hESC enhancer GRCh37_chr16:1592422-1593124 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1542421..1543123) | | |
ID: 127882732 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1583697-1584400 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1533696..1534399) | | |
ID: 127882731 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1582993-1583696 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1532992..1533695) | | |
ID: 127882730 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1545869-1546768 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1495868..1496767) | | |
ID: 127882729 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1544968-1545868 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1494967..1495867) | | |
ID: 126862260 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr16:1574508-1575707 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1524507..1525706) | | |
ID: 105371046 | uncharacterized LOC105371046 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1580527..1610328) | | |
ID: 79652 | transmembrane protein 204 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1528678..1555568) | C16orf30, CLP24 | 611002 |
ID: 57585 | cramped chromatin regulator homolog 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1612360..1677908) | CRAMP1L, HN1L, TCE4 | |
ID: 9894 | telomere maintenance 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1493360..1510454) | CLK2, TEL2, YHFS | 611140 |
ID: 9742 | intraflagellar transport 140 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1510427..1612072, complement) | MZSDS, RP80, SRTD9, WDTC2, c305C8.4, c380F5.1, gs114 | 614620 |