| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134646566-134646904 | Common:7; Rare:109 | ||||
| chr7:134986383-134986556 | Common:4; Rare:66 | ||||
| chr7:135170685-135170965 | Common:3; Rare:92 | ||||
| chr7:135662330-135662520 | Common:4; Rare:79 | ||||
| chr7:139109342-139109495 | Common:1; Rare:46 | ||||
| chr7:139133675-139133833 | Rare:42 | ||||
| chr7:139359672-139359982 | Common:3; Rare:123 | ||||
| chr7:141551284-141551434 | Common:1; Rare:44; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:143380907-143381061 | Rare:38 | ||||
| chr7:143902136-143902304 | Common:5; Rare:52 | ||||
| chr7:148698588-148698932 | Common:2; Rare:125 | ||||
| chr7:149028627-149028938 | Common:2; Rare:101 | ||||
| chr7:149126256-149126408 | Common:6; Rare:49 | ||||
| chr7:149239465-149239672 | Rare:46 | ||||
| chr7:151057856-151058190 | Common:3; Rare:96 |