| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105552408-105552759 | Rare:57 | ||||
| chr4:105708628-105708870 | Common:2; Rare:79 | ||||
| chr4:105895313-105895667 | Rare:102 | ||||
| chr4:105895802-105895879 | Rare:10 | ||||
| chr4:105895956-105896075 | Common:2; Rare:32 | ||||
| chr4:105896093-105896354 | Common:2; Rare:48 | ||||
| chr4:105897507-105897748 | Common:1; Rare:45 | ||||
| chr4:105897879-105898056 | Common:1; Rare:63 | ||||
| chr4:106315445-106315586 | Common:2; Rare:27 | ||||
| chr4:106316173-106316621 | Common:5; Rare:142 | ||||
| chr4:107720175-107720544 | Common:7; Rare:151 | ||||
| chr4:107824461-107824754 | Common:1; Rare:59 | ||||
| chr4:107824769-107825081 | Common:1; Rare:94 | ||||
| chr4:107989661-107989988 | Common:6; Rare:141; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620365-108620647 | Common:6; Rare:141 |