Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151876230-151876630 | Common:5; Rare:199; Clinvar:8; Clinvar (benign):10 | ||||
| chr7:151877112-151877248 | Common:2; Rare:40; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152025531-152025809 | Common:1; Rare:110 | ||||
| chr7:152435901-152436256 | Rare:120 | ||||
| chr7:152676059-152676329 | Common:2; Rare:119; Clinvar:1; Clinvar (benign):12 | ||||
| chr7:152759627-152759846 | Common:4; Rare:83 | ||||
| chr7:155002922-155003561 | Common:12; Rare:218 | ||||
| chr7:155297570-155297973 | Common:6; Rare:163 | ||||
| chr7:155298971-155299211 | Rare:50 | ||||
| chr7:155644280-155644444 | Common:2; Rare:49 | ||||
| chr7:155644560-155644730 | Common:1; Rare:78 | ||||
| chr7:156640526-156640806 | Common:4; Rare:132 | ||||
| chr7:156893108-156893661 | Common:5; Rare:195; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:156949570-156949801 | Common:3; Rare:89 | ||||
| chr7:157010612-157010918 | Common:5; Rare:96 |
- 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