Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88785142-88785328 | Common:2; Rare:73 | ||||
| chr16:88785520-88785830 | Rare:83 | ||||
| chr16:88802643-88802998 | Common:9; Rare:85 | ||||
| chr16:88803453-88803832 | Common:6; Rare:157 | ||||
| chr16:88804581-88804760 | Rare:100; Clinvar (benign):1 | ||||
| chr16:88811412-88811563 | Common:1; Rare:57 | ||||
| chr16:88811880-88812160 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr16:88856918-88857201 | Common:4; Rare:140; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88941307-88941454 | Rare:38 | ||||
| chr16:89093751-89093954 | Common:4; Rare:92 | ||||
| chr16:89201622-89201999 | Common:4; Rare:131 | ||||
| chr16:89217554-89217773 | Common:1; Rare:111 | ||||
| chr16:89489172-89489350 | Common:6; Rare:89 | ||||
| chr16:89490518-89491000 | Common:6; Rare:174 | ||||
| chr16:89508253-89508470 | Common:2; Rare:123; Clinvar:2; Clinvar (benign):2; 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