| ID: 127886692 | H3K4me1 hESC enhancer GRCh37_chr17:36887390-36887927 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38731137..38731674) | | |
| ID: 127886691 | H3K4me1 hESC enhancer GRCh37_chr17:36881911-36882602 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38725658..38726349) | | |
| ID: 127886690 | H3K4me1 hESC enhancer GRCh37_chr17:36873639-36874298 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38717386..38718045) | | |
| ID: 127886689 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:36872979-36873638 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38716726..38717385) | | |
| ID: 127886688 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:36858367-36858898 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38702114..38702645) | | |
| ID: 127886687 | H3K27ac hESC enhancer GRCh37_chr17:36829618-36830453 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38673365..38674200) | | |
| ID: 125177466 | Sharpr-MPRA regulatory region 8107 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38671796..38672090) | | |
| ID: 124903993 | uncharacterized LOC124903993 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38714140..38715667, complement) | | |
| ID: 121587589 | Sharpr-MPRA regulatory region 4536 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38677056..38677350) | | |
| ID: 108004529 | control region 19 heart enhancer [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38728738..38728960) | | |
| ID: 105371763 | uncharacterized LOC105371763 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38701144..38704744) | | |
| ID: 105371762 | uncharacterized LOC105371762 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38719088..38720319, complement) | | |
| ID: 100873688 | RNA, 5S ribosomal pseudogene 440 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38731802..38731920, complement) | RN5S440 | |
| ID: 100616203 | microRNA 4734 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38702262..38702331, complement) | mir-4734 | |
| ID: 100616153 | microRNA 4726 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38719691..38719748) | | |
| ID: 100170841 | elongin BC and polycomb repressive complex 2 associated protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38671703..38674957, complement) | C17orf96, PRR28 | 617795 |
| ID: 284106 | CDGSH iron sulfur domain 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38730341..38735605) | MiNT, Miner2 | 611933 |
| ID: 4302 | MLLT6, PHD finger containing [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38705273..38729795) | AF17 | 600328 |