| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122379367-122379533 | Rare:55 | ||||
| chr4:122732436-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922550-122922633 | Common:2; Rare:53 | ||||
| chr4:122922902-122923137 | Common:2; Rare:67 | ||||
| chr4:123396692-123396847 | Rare:42 | ||||
| chr4:123399338-123399653 | Common:1; Rare:96 | ||||
| chr4:127880797-127880929 | Rare:45 | ||||
| chr4:128061002-128061348 | Common:1; Rare:124 | ||||
| chr4:128811174-128811292 | Rare:23 | ||||
| chr4:129093447-129093748 | Common:2; Rare:86 | ||||
| chr4:133149087-133149294 | Common:2; Rare:60 | ||||
| chr4:137532379-137532694 | Common:2; Rare:52 | ||||
| chr4:139301291-139301543 | Common:4; Rare:76 | ||||
| chr4:139302460-139302719 | Common:2; Rare:52 | ||||
| chr4:139453693-139453745 | Common:2; Rare:12 |