| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139016191-139016293 | Rare:20 | ||||
| chr4:139083420-139084235 | Common:4; Rare:446 | ||||
| chr4:139084154-139084587 | Common:19; Rare:874 | ||||
| chr4:139176361-139177057 | Common:1; Rare:222 | ||||
| chr4:139177109-139177587 | Rare:437 | ||||
| chr4:139295169-139296151 | Common:10; Rare:520 | ||||
| chr4:139300397-139300797 | Rare:58 | ||||
| chr4:139301016-139301702 | Common:38; Rare:817 | ||||
| chr4:139301772-139302750 | Common:30; Rare:745 | ||||
| chr4:139453105-139454254 | Common:34; Rare:1182; Clinvar:53; Clinvar (benign):25 | ||||
| chr4:139555321-139556219 | Common:4; Rare:314 | ||||
| chr4:139556176-139556710 | Common:1; Rare:266 | ||||
| chr4:139557051-139557451 | Common:5; Rare:71 | ||||
| chr4:139606524-139606924 | Common:2; Rare:104 | ||||
| chr4:139665169-139665569 | Common:2; Rare:104 |