| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39638815-39639169 | Common:1; Rare:124 | ||||
| chr4:39697931-39698185 | Common:2; Rare:110 | ||||
| chr4:40056655-40056957 | Common:4; Rare:94 | ||||
| chr4:41256728-41257001 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41261724-41261922 | Rare:76; Clinvar:1 | ||||
| chr4:41934981-41935195 | Common:3; Rare:59 | ||||
| chr4:41990412-41990572 | Common:1; Rare:59 | ||||
| chr4:44678382-44678473 | Rare:28 | ||||
| chr4:44678630-44678707 | Rare:35 | ||||
| chr4:44726547-44726636 | Rare:36 | ||||
| chr4:46123992-46124187 | Common:3; Rare:34 | ||||
| chr4:46124316-46124341 | Rare:6 | ||||
| chr4:46993443-46993895 | Common:2; Rare:113 | ||||
| chr4:47463647-47463817 | Common:2; Rare:56 | ||||
| chr4:47485208-47485340 | Common:1; Rare:49 |