Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128067213-128067591 | Common:13; Rare:215 | ||||
| chr9:128067746-128068371 | Common:6; Rare:417 | ||||
| chr9:128098289-128098601 | Common:4; Rare:147 | ||||
| chr9:128127485-128127964 | Common:13; Rare:346 | ||||
| chr9:128127877-128128278 | Common:20; Rare:284 | ||||
| chr9:128128318-128128626 | Common:6; Rare:320 | ||||
| chr9:128159939-128160444 | Common:8; Rare:324 | ||||
| chr9:128190439-128190738 | Rare:145 | ||||
| chr9:128191435-128191971 | Common:6; Rare:377 | ||||
| chr9:128202910-128203439 | Common:4; Rare:177; Clinvar (benign):1 | ||||
| chr9:128218700-128219090 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:128250351-128250763 | Rare:245; Clinvar (benign):6 | ||||
| chr9:128275580-128276403 | Common:17; Rare:705 | ||||
| chr9:128322346-128323015 | Common:14; Rare:609; Clinvar:9; Clinvar (benign):23; Clinvar (pathogenic):5 | ||||
| chr9:128339970-128340838 | Common:16; Rare:653 |
- 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