Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132369851-132369977 | Common:3; Rare:45; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:132387666-132387845 | Common:1; Rare:32 | ||||
| chr5:132410567-132410945 | Common:1; Rare:76 | ||||
| chr5:132411022-132411189 | Common:2; Rare:42 | ||||
| chr5:132419710-132419902 | Common:1; Rare:47 | ||||
| chr5:132490295-132490537 | Common:2; Rare:66 | ||||
| chr5:132490754-132491030 | Rare:70 | ||||
| chr5:132556735-132557046 | Common:1; Rare:95; Clinvar:1 | ||||
| chr5:132557549-132557652 | Common:1; Rare:23 | ||||
| chr5:132737472-132737751 | Rare:90 | ||||
| chr5:132776080-132776550 | Common:2; Rare:83 | ||||
| chr5:132807426-132807591 | Rare:32 | ||||
| chr5:132830593-132830804 | Rare:57 | ||||
| chr5:132866415-132866716 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963569-132963840 | Common:1; Rare:71 |
- 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