Proximal
SK-N-SH(Human) | 7944 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8248029-8248182 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8295311-8295538 | Common:1; Rare:58 | ||||
| chr17:8382746-8382952 | Common:2; Rare:36 | ||||
| chr17:8383075-8383426 | Rare:109 | ||||
| chr17:8383589-8383729 | Common:1; Rare:32 | ||||
| chr17:10697262-10697655 | Common:5; Rare:169; Clinvar:7; Clinvar (benign):7 | ||||
| chr17:11997414-11997607 | Rare:70 | ||||
| chr17:13601909-13602213 | Common:3; Rare:93 | ||||
| chr17:14069347-14069580 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:14300904-14301103 | Common:2; Rare:66 | ||||
| chr17:15260746-15260861 | Rare:46; Clinvar (benign):3 | ||||
| chr17:15999505-16000143 | Common:4; Rare:265; Clinvar:7; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr17:16058295-16058556 | Common:1; Rare:53 | ||||
| chr17:16080296-16080476 | Common:1; Rare:37 | ||||
| chr17:16215364-16215639 | Common:2; Rare:114 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box