ID: 127885846 | H3K4me1 hESC enhancer GRCh37_chr17:15313079-15313579 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15409762..15410262) | | |
ID: 126862513 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:15181646-15182845 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15278329..15279528) | | |
ID: 124903932 | uncharacterized LOC124903932 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15289263..15312023) | | |
ID: 124903931 | uncharacterized LOC124903931 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15260959..15265909) | | |
ID: 107105254 | RNA, U6 small nuclear 799, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15311346..15311452) | | |
ID: 106479509 | RNA, 7SL, cytoplasmic 792, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15408384..15408688) | | |
ID: 100616125 | microRNA 4731 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15251627..15251696, complement) | | |
ID: 64518 | tektin 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15303812..15343671, complement) | SPGF81 | 612683 |
ID: 5376 | peripheral myelin protein 22 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15229779..15265326, complement) | CIDP, CMT1A, CMT1E, DSS, GAS-3, GAS3, HMSNIA, HNPP, Sp110 | 601097 |