Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:116755690-116755981 | Common:2; Rare:346 | ||||
| chr8:116766207-116766635 | Common:12; Rare:296 | ||||
| chr8:116766900-116767398 | Common:4; Rare:158 | ||||
| chr8:116873456-116874544 | Common:13; Rare:509 | ||||
| chr8:116874606-116875009 | Common:16; Rare:429; Clinvar (benign):1 | ||||
| chr8:116937958-116938250 | Common:3; Rare:128 | ||||
| chr8:116938307-116938626 | Common:18; Rare:244 | ||||
| chr8:117520490-117520846 | Common:17; Rare:212 | ||||
| chr8:118110701-118111215 | Common:2; Rare:265; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:118111686-118112118 | Common:6; Rare:314; Clinvar:5; Clinvar (benign):9 | ||||
| chr8:118621801-118622350 | Common:30; Rare:378 | ||||
| chr8:118951210-118951740 | Common:6; Rare:151 | ||||
| chr8:118951763-118952229 | Common:6; Rare:296; Clinvar:17; Clinvar (benign):6 | ||||
| chr8:118952180-118952580 | Rare:119 | ||||
| chr8:119208140-119208584 | Common:21; Rare:416 |
- 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