Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:135181007-135181526 | Common:4; Rare:335 | ||||
| chr6:135181573-135181840 | Common:3; Rare:60 | ||||
| chr6:135497180-135497602 | Common:1; Rare:141; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:135497569-135498031 | Common:11; Rare:315; Clinvar:4; Clinvar (benign):5 | ||||
| chr6:136250178-136250646 | Common:7; Rare:224 | ||||
| chr6:136289372-136289510 | Rare:63 | ||||
| chr6:136289717-136290304 | Common:5; Rare:464 | ||||
| chr6:136550339-136550924 | Common:7; Rare:367 | ||||
| chr6:136792000-136792793 | Common:18; Rare:446 | ||||
| chr6:136792994-136793270 | Common:2; Rare:134 | ||||
| chr6:136822444-136823330 | Common:22; Rare:526; Clinvar:25; Clinvar (benign):11; Clinvar (pathogenic):9 | ||||
| chr6:137044110-137044305 | Common:2; Rare:45 | ||||
| chr6:137219310-137219549 | Common:6; Rare:138; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:137866922-137867306 | Rare:239 | ||||
| chr6:138107076-138107733 | Common:15; Rare:423 |
- 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