| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145619040-145619590 | Common:4; Rare:253; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:146175647-146175809 | Common:1; Rare:59 | ||||
| chr4:146522283-146522475 | Common:9; Rare:128 | ||||
| chr4:147617202-147617479 | Common:2; Rare:114 | ||||
| chr4:147684077-147684306 | Common:2; Rare:160 | ||||
| chr4:147731916-147732162 | Common:1; Rare:126 | ||||
| chr4:148442291-148443054 | Common:1; Rare:261; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150078480-150079000 | Common:7; Rare:194 | ||||
| chr4:151015116-151015451 | Rare:124 | ||||
| chr4:151015688-151015884 | Rare:176 | ||||
| chr4:151099481-151099835 | Common:6; Rare:179 | ||||
| chr4:151325467-151325727 | Common:2; Rare:80 | ||||
| chr4:151408833-151409304 | Common:11; Rare:266 | ||||
| chr4:151760924-151761189 | Rare:164 | ||||
| chr4:152536032-152536487 | Common:5; Rare:293 |