| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:3292771-3293079 | Common:2; Rare:121 | ||||
| chr4:3463151-3463374 | Common:3; Rare:75; Clinvar (benign):2 | ||||
| chr4:3532279-3532653 | Common:2; Rare:177 | ||||
| chr4:4248198-4248272 | Common:1; Rare:32 | ||||
| chr4:4290097-4290300 | Common:4; Rare:85 | ||||
| chr4:4541957-4542347 | Common:4; Rare:138 | ||||
| chr4:5019441-5019529 | Rare:34 | ||||
| chr4:6640515-6640762 | Common:3; Rare:97 | ||||
| chr4:6709793-6709974 | Rare:55 | ||||
| chr4:6909365-6909473 | Rare:30 | ||||
| chr4:6909684-6909855 | Rare:68 | ||||
| chr4:6987006-6987303 | Common:2; Rare:94 | ||||
| chr4:7068019-7068374 | Common:7; Rare:121 | ||||
| chr4:8198950-8199371 | Common:2; Rare:111 | ||||
| chr4:8269612-8269757 | Common:1; Rare:56 |