Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:112205590-112205815 | Common:3; Rare:43 | ||||
chr7:116211453-116211605 | Rare:33 | ||||
chr7:116239230-116239262 | Rare:5 | ||||
chr7:128853749-128854033 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):3 | ||||
chr7:128858003-128858486 | Common:2; Rare:121; Clinvar:10; Clinvar (benign):14 | ||||
chr7:130541029-130541218 | Rare:49 | ||||
chr7:130894381-130894485 | Common:1; Rare:19 | ||||
chr7:130912173-130912369 | Common:1; Rare:33 | ||||
chr7:130930510-130930630 | Common:1; Rare:15 | ||||
chr7:131106384-131106543 | Rare:31 | ||||
chr7:131107385-131107447 | Rare:8 | ||||
chr7:131107947-131108205 | Common:1; Rare:42 | ||||
chr7:134867567-134867800 | Common:1; Rare:51 | ||||
chr7:134957878-134958112 | Common:1; Rare:35 | ||||
chr7:143388537-143388944 | Common:6; Rare:136 |