| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17614578-17614657 | Common:1; Rare:36 | ||||
| chr4:17810681-17810973 | Common:1; Rare:91 | ||||
| chr4:20700314-20700441 | Rare:47 | ||||
| chr4:23889957-23890134 | Rare:31 | ||||
| chr4:24584435-24584696 | Rare:85 | ||||
| chr4:24795348-24795592 | Common:1; Rare:61 | ||||
| chr4:25160411-25160727 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:26320900-26321041 | Rare:49; Clinvar (benign):1 | ||||
| chr4:30721984-30722169 | Common:1; Rare:57 | ||||
| chr4:37826505-37826735 | Common:6; Rare:83 | ||||
| chr4:37890992-37891093 | Common:1; Rare:31 | ||||
| chr4:39458876-39459111 | Common:2; Rare:131; Clinvar (benign):5 | ||||
| chr4:39527426-39527754 | Common:2; Rare:82 | ||||
| chr4:39527951-39528029 | Rare:20 | ||||
| chr4:39638847-39639169 | Common:1; Rare:117 |