| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112636907-112637187 | Common:1; Rare:77 | ||||
| chr4:120066775-120066904 | Common:1; Rare:40 | ||||
| chr4:122922987-122923106 | Common:1; Rare:33 | ||||
| chr4:139453788-139454213 | Common:3; Rare:115; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373392-140373704 | Common:2; Rare:129 | ||||
| chr4:140756343-140756414 | Rare:17 | ||||
| chr4:143184616-143184922 | Common:9; Rare:121 | ||||
| chr4:144645708-144645767 | Common:1; Rare:17 | ||||
| chr4:144645882-144646424 | Common:4; Rare:126 | ||||
| chr4:144646700-144646948 | Rare:76 | ||||
| chr4:145098156-145098363 | Rare:74 | ||||
| chr4:145482762-145482788 | Rare:8 | ||||
| chr4:145482861-145483044 | Rare:36 | ||||
| chr4:152679931-152680161 | Rare:56 | ||||
| chr4:152779747-152780179 | Common:2; Rare:106 |