| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139453683-139454202 | Common:5; Rare:142; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556106-139556656 | Rare:110 | ||||
| chr4:140373384-140373696 | Common:2; Rare:126 | ||||
| chr4:140523967-140524226 | Common:2; Rare:76 | ||||
| chr4:140756139-140756474 | Common:1; Rare:70 | ||||
| chr4:143184646-143185112 | Common:9; Rare:175 | ||||
| chr4:143336573-143336912 | Rare:78 | ||||
| chr4:143381866-143381973 | Rare:17 | ||||
| chr4:143513336-143513759 | Common:2; Rare:135 | ||||
| chr4:144645844-144646156 | Common:1; Rare:91 | ||||
| chr4:145098141-145098361 | Rare:77 | ||||
| chr4:145619346-145619406 | Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147480706-147480977 | Rare:42 | ||||
| chr4:147617218-147617463 | Common:1; Rare:57 | ||||
| chr4:147684096-147684256 | Common:1; Rare:62 |