| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82429377-82429644 | Common:1; Rare:160; Clinvar:11; Clinvar (benign):6 | ||||
| chr4:82430678-82430825 | Common:1; Rare:55 | ||||
| chr4:82891031-82891317 | Common:1; Rare:111 | ||||
| chr4:82900454-82900805 | Rare:111 | ||||
| chr4:83455787-83456078 | Common:2; Rare:110 | ||||
| chr4:83485065-83485287 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:84966623-84966995 | Rare:97 | ||||
| chr4:85827814-85827937 | Rare:17 | ||||
| chr4:85929800-85930016 | Common:1; Rare:43 | ||||
| chr4:86360049-86360172 | Rare:24; Clinvar:1 | ||||
| chr4:86594060-86594353 | Rare:95 | ||||
| chr4:86936177-86936330 | Rare:35 | ||||
| chr4:87422528-87422640 | Common:1; Rare:33 | ||||
| chr4:87529022-87529523 | Common:5; Rare:89 | ||||
| chr4:87531042-87531121 | Rare:16 |