Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12288918-12289075 | Rare:34 | ||||
| chr3:12484164-12484521 | Common:4; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12556830-12557170 | Common:5; Rare:100 | ||||
| chr3:12664064-12664469 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:12759269-12759411 | Common:1; Rare:35 | ||||
| chr3:12759494-12759670 | Common:4; Rare:20 | ||||
| chr3:12841477-12841896 | Common:2; Rare:133 | ||||
| chr3:12967622-12968032 | Common:5; Rare:147 | ||||
| chr3:12994700-12994824 | Rare:20 | ||||
| chr3:12995019-12995282 | Common:1; Rare:62 | ||||
| chr3:13420242-13420415 | Common:1; Rare:48 | ||||
| chr3:13479965-13480345 | Common:3; Rare:95 | ||||
| chr3:14124329-14124439 | Common:1; Rare:32 | ||||
| chr3:14124848-14125160 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178539-14178926 | Common:2; Rare:203; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 |
- 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