| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139302460-139302528 | Rare:12 | ||||
| chr4:139453674-139453749 | Common:2; Rare:24 | ||||
| chr4:139453766-139454210 | Common:3; Rare:119; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373384-140373701 | Common:2; Rare:129 | ||||
| chr4:140523931-140524231 | Common:2; Rare:93 | ||||
| chr4:142305805-142306025 | Common:1; Rare:28 | ||||
| chr4:143184840-143184914 | Common:6; Rare:32 | ||||
| chr4:143337091-143337206 | Rare:47 | ||||
| chr4:143381866-143382005 | Rare:20 | ||||
| chr4:143513348-143513538 | Common:2; Rare:68 | ||||
| chr4:143700096-143700234 | Rare:38 | ||||
| chr4:143905557-143905580 | Rare:4 | ||||
| chr4:144645866-144646187 | Common:1; Rare:93 | ||||
| chr4:144646343-144646723 | Common:1; Rare:86 | ||||
| chr4:145098141-145098374 | Rare:81 |