Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:154510515-154510908 | Common:3; Rare:120 | ||||
| chr6:154733243-154733428 | Rare:74 | ||||
| chr6:154733913-154734328 | Common:5; Rare:130 | ||||
| chr6:154995001-154995393 | Common:7; Rare:153 | ||||
| chr6:155314418-155314922 | Common:16; Rare:167 | ||||
| chr6:156777382-156777681 | Common:1; Rare:91 | ||||
| chr6:156777727-156777970 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:156778324-156778702 | Common:3; Rare:129; Clinvar:5; Clinvar (benign):5 | ||||
| chr6:156778810-156778970 | Common:3; Rare:73; Clinvar:6; Clinvar (benign):11 | ||||
| chr6:156779885-156780043 | Common:3; Rare:39 | ||||
| chr6:157148540-157149380 | Common:2; Rare:191; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:157323134-157323308 | Rare:32 | ||||
| chr6:157323462-157323662 | Common:3; Rare:72 | ||||
| chr6:157324034-157324163 | Common:1; Rare:21 | ||||
| chr6:157380985-157381238 | Common:2; Rare:82 |
- 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