Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:892520-893002 | Common:5; Rare:155 | ||||
| chr5:1111980-1112145 | Rare:61 | ||||
| chr5:1294920-1295270 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:1345045-1345232 | Common:2; Rare:69 | ||||
| chr5:1524248-1524366 | Rare:34 | ||||
| chr5:1799797-1799999 | Common:4; Rare:97 | ||||
| chr5:1801285-1801454 | Common:4; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:1882511-1882678 | Common:1; Rare:57; Clinvar:1 | ||||
| chr5:1882810-1883190 | Common:5; Rare:71 | ||||
| chr5:5422224-5422759 | Common:3; Rare:186 | ||||
| chr5:6378472-6378760 | Rare:110 | ||||
| chr5:6632994-6633461 | Common:8; Rare:151; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:6712756-6713530 | Common:9; Rare:264 | ||||
| chr5:7868947-7869245 | Common:2; Rare:160; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:10249810-10250333 | Common:19; Rare:261; Clinvar:3; 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