Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:76152405-76152576 | Common:3; Rare:30 | ||||
| chr14:76375993-76376127 | Common:2; Rare:13 | ||||
| chr14:76812814-76813188 | Common:2; Rare:118 | ||||
| chr14:77028628-77028973 | Rare:109 | ||||
| chr14:77097873-77098338 | Rare:142 | ||||
| chr14:77181649-77181883 | Common:2; Rare:56 | ||||
| chr14:77182077-77182352 | Common:2; Rare:49 | ||||
| chr14:77320294-77320485 | Common:2; Rare:61; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr14:77320820-77321131 | Rare:99; Clinvar:3 | ||||
| chr14:77321273-77321446 | Common:4; Rare:91 | ||||
| chr14:77376996-77377211 | Common:4; Rare:74 | ||||
| chr14:77377280-77377550 | Common:3; Rare:90 | ||||
| chr14:77457489-77457903 | Common:2; Rare:123 | ||||
| chr14:77457950-77458138 | Rare:49 | ||||
| chr14:77616583-77617132 | Common:3; Rare:155; Clinvar:3; Clinvar (benign):5 |
- 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