Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100200666-100200891 | Common:2; Rare:73 | ||||
| chr12:100266935-100267277 | Common:2; Rare:165 | ||||
| chr12:100573522-100573765 | Rare:80 | ||||
| chr12:100573840-100574420 | Common:6; Rare:139 | ||||
| chr12:101280009-101280183 | Common:1; Rare:54 | ||||
| chr12:101407493-101408326 | Common:3; Rare:202 | ||||
| chr12:101697394-101697690 | Common:2; Rare:88 | ||||
| chr12:101697750-101698000 | Common:1; Rare:78 | ||||
| chr12:101830360-101830750 | Common:5; Rare:118; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr12:101830799-101831186 | Common:2; Rare:121; Clinvar (benign):2 | ||||
| chr12:101877399-101877784 | Common:4; Rare:101 | ||||
| chr12:102061920-102062310 | Common:1; Rare:103 | ||||
| chr12:102120034-102120568 | Common:4; Rare:166 | ||||
| chr12:102917293-102917534 | Common:3; Rare:63 | ||||
| chr12:102917580-102918100 | Common:6; Rare:90; Clinvar (benign):2 |
- 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