| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121870406-121870719 | Common:1; Rare:78; Clinvar (benign):1 | ||||
| chr4:122732428-122732762 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922932-122923139 | Common:2; Rare:63 | ||||
| chr4:127880778-127880934 | Rare:53 | ||||
| chr4:128060994-128061325 | Common:1; Rare:118 | ||||
| chr4:128811243-128811317 | Rare:16 | ||||
| chr4:128811338-128811345 | Rare:3 | ||||
| chr4:129093475-129093736 | Common:1; Rare:78 | ||||
| chr4:138242342-138242646 | Common:1; Rare:64 | ||||
| chr4:139084192-139084554 | Common:4; Rare:157 | ||||
| chr4:139301232-139301543 | Common:4; Rare:87 | ||||
| chr4:139453693-139453718 | Common:1; Rare:4 | ||||
| chr4:139454011-139454190 | Common:2; Rare:47; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:139556158-139556310 | Rare:35 | ||||
| chr4:140154136-140154288 | Rare:61 |