| ID: 127887679 | H3K4me1 hESC enhancer GRCh37_chr17:65049323-65050167 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67053207..67054051) | | |
| ID: 127887678 | H3K4me1 hESC enhancer GRCh37_chr17:65002313-65002813 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67006197..67006697) | | |
| ID: 127887677 | H3K4me1 hESC enhancer GRCh37_chr17:65001812-65002312 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67005696..67006196) | | |
| ID: 127887676 | H3K4me1 hESC enhancer GRCh37_chr17:64979083-64979584 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66982967..66983468) | | |
| ID: 127887675 | H3K4me1 hESC enhancer GRCh37_chr17:64972550-64973503 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66976434..66977387) | | |
| ID: 127887674 | H3K4me1 hESC enhancer GRCh37_chr17:64971595-64972549 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66975479..66976433) | | |
| ID: 126862622 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:65103924-65105123 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67107808..67109007) | | |
| ID: 121603771 | H3K27ac-H3K4me1 hESC enhancers GRCh37_chr17:64974248-64974825 and GRCh37_chr17:64974826-64975402 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66978132..66979286) | | |
| ID: 100873692 | RNA, 5S ribosomal pseudogene 446 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66895491..66895572) | RN5S446 | |
| ID: 27092 | calcium voltage-gated channel auxiliary subunit gamma 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66964707..67033398) | | 606404 |
| ID: 27091 | calcium voltage-gated channel auxiliary subunit gamma 5 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66835117..66894751) | | 606405 |
| ID: 9931 | helicase with zinc finger [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67070444..67245989, complement) | DHRC, DRHC, HUMORF5 | 606699 |
| ID: 786 | calcium voltage-gated channel auxiliary subunit gamma 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67044554..67056797) | CACNLG | 114209 |