ID: 132090370 | Neanderthal introgressed variant-containing enhancer experimental_42864 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1505887..1506056) | | |
ID: 130058167 | ATAC-STARR-seq lymphoblastoid active region 10226 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1493018..1493067) | | |
ID: 129663721 | ReSE screen-validated silencer GRCh37_chr16:1609654-1609839 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1559653..1559838) | | |
ID: 129663720 | ReSE screen-validated silencer GRCh37_chr16:1534269-1534471 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1484268..1484470) | | |
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: 127882728 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1543166-1544066 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1493165..1494065) | | |
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: 390667 | pentraxin 4 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1485886..1488944, complement) | C16orf38 | 613442 |
ID: 79652 | transmembrane protein 204 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1528678..1555568) | C16orf30, CLP24 | 611002 |
ID: 64725 | RPS3A pseudogene 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1477983..1478590) | RPS3A_21_1466 | |
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 |