Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35745347-35745685 | Rare:106 | ||||
| chr19:35748248-35748664 | Common:3; Rare:118 | ||||
| chr19:35757841-35758229 | Common:2; Rare:120 | ||||
| chr19:35775314-35775604 | Common:1; Rare:81 | ||||
| chr19:35845437-35845734 | Common:2; Rare:98; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr19:35851183-35851583 | Common:6; Rare:173; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
| chr19:35868439-35868579 | Rare:39 | ||||
| chr19:35899662-35899896 | Common:1; Rare:62 | ||||
| chr19:35900513-35900742 | Common:1; Rare:55 | ||||
| chr19:35994997-35995248 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr19:36008736-36008916 | Rare:37 | ||||
| chr19:36014169-36014604 | Common:2; Rare:117 | ||||
| chr19:36054049-36054191 | Rare:59 | ||||
| chr19:36054750-36054913 | Rare:48 | ||||
| chr19:36055111-36055511 | Common:4; Rare:120; Clinvar:1; Clinvar (benign):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