| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119454561-119454904 | Common:16; Rare:117 | ||||
| chr4:119501238-119501264 | Rare:7 | ||||
| chr4:119504537-119504746 | Common:1; Rare:45 | ||||
| chr4:119515976-119516099 | Rare:12 | ||||
| chr4:124020161-124020359 | Common:1; Rare:34 | ||||
| chr4:139387685-139387965 | Common:1; Rare:52 | ||||
| chr4:148101304-148101361 | Common:1; Rare:11 | ||||
| chr4:150583558-150583625 | Rare:16 | ||||
| chr4:153684072-153684309 | Common:1; Rare:74 | ||||
| chr4:168903483-168903788 | Rare:55 | ||||
| chr4:168904860-168904997 | Common:3; Rare:21 | ||||
| chr4:168924102-168924418 | Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:173391382-173391506 | Rare:33 | ||||
| chr5:1633919-1634049 | Common:2; Rare:43 | ||||
| chr5:1930949-1931282 | Common:3; Rare:85 |