| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:54231857-54232074 | Common:2; Rare:50 | ||||
| chr4:54233022-54233169 | Common:3; Rare:36 | ||||
| chr4:55397875-55398029 | Common:2; Rare:34 | ||||
| chr4:55398134-55398348 | Common:2; Rare:39 | ||||
| chr4:55400600-55400725 | Common:1; Rare:17 | ||||
| chr4:55405323-55405420 | Rare:16 | ||||
| chr4:55419133-55419513 | Common:1; Rare:60 | ||||
| chr4:55947962-55948253 | Common:1; Rare:51 | ||||
| chr4:56354718-56354996 | Common:2; Rare:57 | ||||
| chr4:56490341-56490917 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:56497780-56497936 | Common:1; Rare:20 | ||||
| chr4:57008660-57008891 | Common:2; Rare:40 | ||||
| chr4:57031287-57031445 | Common:2; Rare:36 | ||||
| chr4:57101685-57101775 | Rare:16 | ||||
| chr4:60683451-60683640 | Common:3; Rare:35 |