| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134646566-134646897 | Common:6; Rare:107 | ||||
| chr7:134779302-134779740 | Rare:71 | ||||
| chr7:134891315-134891621 | Common:3; Rare:75 | ||||
| chr7:134986448-134986664 | Common:5; Rare:72 | ||||
| chr7:135170387-135170509 | Rare:42 | ||||
| chr7:135170645-135170999 | Common:6; Rare:112 | ||||
| chr7:135211488-135211740 | Common:2; Rare:119 | ||||
| chr7:135662383-135662556 | Common:3; Rare:85 | ||||
| chr7:135976901-135976979 | Rare:23 | ||||
| chr7:135977019-135977119 | Rare:22 | ||||
| chr7:135977121-135977481 | Common:3; Rare:137 | ||||
| chr7:136868422-136868492 | Rare:15 | ||||
| chr7:136868528-136868909 | Common:1; Rare:78 | ||||
| chr7:136868964-136869294 | Common:2; Rare:68; Clinvar (benign):3 | ||||
| chr7:137454810-137455223 | Common:1; Rare:92 |