| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:128287779-128288057 | Common:3; Rare:106 | ||||
| chr4:128810213-128810237 | Rare:6 | ||||
| chr4:128811096-128811341 | Rare:52 | ||||
| chr4:129093468-129093753 | Common:1; Rare:85 | ||||
| chr4:137532346-137532657 | Common:2; Rare:51 | ||||
| chr4:139177175-139177456 | Rare:83 | ||||
| chr4:139301301-139301562 | Common:3; Rare:81 | ||||
| chr4:139302460-139302553 | Rare:15 | ||||
| chr4:139453674-139453697 | Common:1; Rare:9 | ||||
| chr4:139453699-139454204 | Common:4; Rare:136; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556100-139556270 | Rare:38 | ||||
| chr4:139556397-139556622 | Rare:32 | ||||
| chr4:139665745-139666022 | Common:2; Rare:59 | ||||
| chr4:140373384-140373709 | Common:3; Rare:133 | ||||
| chr4:140755938-140756478 | Common:1; Rare:131 |