Proximal
MCF 10A(Human) | 31434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37422520-37422764 | Common:7; Rare:113 | ||||
| chr9:37422796-37423004 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr9:37464869-37465109 | Common:4; Rare:64 | ||||
| chr9:37465147-37465606 | Common:3; Rare:145 | ||||
| chr9:37465750-37466141 | Common:3; Rare:93 | ||||
| chr9:37485689-37486109 | Common:4; Rare:142 | ||||
| chr9:37576177-37576463 | Common:1; Rare:68 | ||||
| chr9:37576567-37576601 | Rare:4 | ||||
| chr9:37592172-37592284 | Rare:43 | ||||
| chr9:37592378-37592791 | Common:3; Rare:133 | ||||
| chr9:37753413-37753638 | Common:3; Rare:81 | ||||
| chr9:37753667-37753879 | Common:7; Rare:116 | ||||
| chr9:37753918-37754052 | Common:1; Rare:45 | ||||
| chr9:37784716-37784837 | Rare:47; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:37784838-37785311 | Common:1; Rare:187; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 |
- 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