Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:9924851-9924983 | Common:1; Rare:27 | ||||
| chr17:10697472-10697736 | Common:5; Rare:112; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:11996845-11997036 | Common:1; Rare:47 | ||||
| chr17:11997330-11997636 | Common:3; Rare:116 | ||||
| chr17:12020685-12020887 | Common:2; Rare:85 | ||||
| chr17:12789379-12789567 | Rare:68 | ||||
| chr17:13017928-13018370 | Common:8; Rare:145; Clinvar (benign):2 | ||||
| chr17:14069345-14069593 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:14300788-14301140 | Common:3; Rare:94 | ||||
| chr17:15260281-15260681 | Common:5; Rare:97; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:15260728-15260995 | Common:2; Rare:94; Clinvar (benign):5 | ||||
| chr17:15262531-15262758 | Rare:53 | ||||
| chr17:15563424-15563787 | Common:1; Rare:126 | ||||
| chr17:15651689-15651989 | Rare:53 | ||||
| chr17:15684228-15684357 | Common:3; Rare:43 |
- 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