Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:108079785-108079942 | Common:2; Rare:22 | ||||
chr7:113118526-113118671 | Common:1; Rare:51 | ||||
chr7:116239246-116239424 | Rare:38 | ||||
chr7:128591846-128591879 | Rare:8 | ||||
chr7:128842950-128843304 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
chr7:129410521-129410667 | Common:2; Rare:24 | ||||
chr7:130500306-130500525 | Common:2; Rare:50 | ||||
chr7:130513605-130513807 | Common:1; Rare:37 | ||||
chr7:130514350-130514578 | Common:1; Rare:44 | ||||
chr7:130523640-130523827 | Common:1; Rare:32 | ||||
chr7:130525567-130525601 | Rare:2 | ||||
chr7:130530264-130530446 | Common:1; Rare:42 | ||||
chr7:130531971-130532229 | Rare:61 | ||||
chr7:130532468-130532615 | Common:1; Rare:43 | ||||
chr7:130541131-130541391 | Rare:61 |