| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:113761129-113761263 | Common:1; Rare:33 | ||||
| chr4:118836043-118836204 | Common:1; Rare:33 | ||||
| chr4:119212516-119212738 | Common:3; Rare:58 | ||||
| chr4:119300721-119300745 | Rare:11 | ||||
| chr4:120066778-120066958 | Common:3; Rare:53 | ||||
| chr4:122732432-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922933-122923139 | Common:2; Rare:63 | ||||
| chr4:123396654-123396836 | Rare:46 | ||||
| chr4:123399333-123399653 | Common:1; Rare:98 | ||||
| chr4:127880778-127880929 | Rare:53 | ||||
| chr4:128061002-128061325 | Common:1; Rare:116 | ||||
| chr4:129093444-129093744 | Common:2; Rare:85 | ||||
| chr4:133149090-133149316 | Common:2; Rare:67 | ||||
| chr4:139301295-139301557 | Common:4; Rare:81 | ||||
| chr4:139453758-139454185 | Common:3; Rare:109; Clinvar:10; Clinvar (benign):4 |