| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:8435669-8436282 | Common:6; Rare:247 | ||||
| chr4:8438221-8439070 | Common:7; Rare:210 | ||||
| chr4:8440158-8441011 | Common:3; Rare:747 | ||||
| chr4:8592401-8593578 | Common:28; Rare:650 | ||||
| chr4:10019015-10019488 | Common:6; Rare:204; Clinvar (benign):1 | ||||
| chr4:10096089-10096899 | Common:10; Rare:244 | ||||
| chr4:10106602-10107002 | Rare:206 | ||||
| chr4:10115725-10116186 | Common:18; Rare:415 | ||||
| chr4:10116294-10116694 | Common:1; Rare:208 | ||||
| chr4:10116670-10117210 | Common:65; Rare:1474 | ||||
| chr4:10457234-10457634 | Common:30; Rare:634 | ||||
| chr4:10457683-10458301 | Common:2; Rare:136 | ||||
| chr4:13483499-13484880 | Common:8; Rare:1141 | ||||
| chr4:13544760-13544940 | Common:1; Rare:59 | ||||
| chr4:13544910-13545310 | Common:2; Rare:195 |