| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56435959-56436327 | Rare:134 | ||||
| chr4:56467542-56467704 | Common:2; Rare:68; Clinvar (benign):5 | ||||
| chr4:56977545-56977753 | Common:2; Rare:80 | ||||
| chr4:67545358-67545714 | Common:2; Rare:82 | ||||
| chr4:67701070-67701371 | Common:4; Rare:145 | ||||
| chr4:68349936-68350228 | Common:2; Rare:102 | ||||
| chr4:70688182-70688586 | Common:2; Rare:99 | ||||
| chr4:70902191-70902426 | Common:4; Rare:82 | ||||
| chr4:73258526-73258748 | Common:1; Rare:68 | ||||
| chr4:73869707-73869989 | Common:2; Rare:105 | ||||
| chr4:74038670-74038916 | Rare:67 | ||||
| chr4:74099184-74099440 | Common:2; Rare:61 | ||||
| chr4:74158009-74158179 | Rare:81 | ||||
| chr4:74364988-74365149 | Common:1; Rare:49 | ||||
| chr4:75514282-75514492 | Rare:68 |