Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:129461740-129462100 | Common:7; Rare:155 | ||||
| chr5:129904086-129904496 | Common:3; Rare:103 | ||||
| chr5:131164494-131164827 | Common:4; Rare:126 | ||||
| chr5:131165090-131165498 | Common:7; Rare:362; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr5:131170624-131171054 | Common:4; Rare:263; Clinvar (benign):5 | ||||
| chr5:131263656-131264176 | Common:5; Rare:376 | ||||
| chr5:131264297-131264700 | Common:4; Rare:200 | ||||
| chr5:131635069-131635752 | Common:3; Rare:527 | ||||
| chr5:131796899-131797381 | Rare:324 | ||||
| chr5:132227300-132227630 | Common:2; Rare:71 | ||||
| chr5:132227743-132228086 | Common:7; Rare:176 | ||||
| chr5:132228110-132228320 | Common:2; Rare:47 | ||||
| chr5:132293814-132294540 | Common:5; Rare:351 | ||||
| chr5:132295243-132296236 | Common:4; Rare:188 | ||||
| chr5:132369511-132369991 | Common:29; Rare:426; Clinvar:15; Clinvar (benign):17; Clinvar (pathogenic):6 |
- 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