| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:20252943-20253117 | Rare:42 | ||||
| chr4:20254232-20255514 | Common:8; Rare:426 | ||||
| chr4:20700214-20700466 | Rare:102 | ||||
| chr4:22515186-22515318 | Rare:30 | ||||
| chr4:22515351-22515468 | Common:2; Rare:22 | ||||
| chr4:22515885-22516312 | Common:5; Rare:132 | ||||
| chr4:23890033-23890166 | Rare:20 | ||||
| chr4:24583614-24584014 | Common:1; Rare:129 | ||||
| chr4:24584447-24584765 | Common:1; Rare:91 | ||||
| chr4:24912380-24912780 | Common:5; Rare:112 | ||||
| chr4:24912844-24913062 | Common:1; Rare:73 | ||||
| chr4:25030830-25031280 | Common:1; Rare:112 | ||||
| chr4:25159927-25160136 | Common:1; Rare:58 | ||||
| chr4:25160385-25160741 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233883-25234078 | Rare:87 |