Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46698314-46698714 | Common:10; Rare:186 | ||||
| chr2:46698735-46698955 | Common:1; Rare:61 | ||||
| chr2:46914013-46915064 | Common:4; Rare:232 | ||||
| chr2:46915714-46916180 | Common:4; Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46940660-46940930 | Common:2; Rare:65 | ||||
| chr2:46940950-46941370 | Common:3; Rare:146 | ||||
| chr2:46941682-46941836 | Common:3; Rare:54; Clinvar (benign):1 | ||||
| chr2:47034361-47034584 | Common:3; Rare:45 | ||||
| chr2:47108611-47108923 | Common:2; Rare:82 | ||||
| chr2:47176406-47176966 | Common:7; Rare:257; Clinvar (benign):5 | ||||
| chr2:47345057-47345354 | Common:1; Rare:83 | ||||
| chr2:47369003-47369354 | Common:3; Rare:134; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:47402893-47403202 | Common:1; Rare:142; Clinvar:46; Clinvar (benign):30; Clinvar (pathogenic):1 | ||||
| chr2:47782864-47783218 | Common:3; Rare:154; Clinvar:6; Clinvar (benign):13 | ||||
| chr2:47783751-47784025 | Common:6; Rare:65; 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