| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38867710-38867814 | Common:1; Rare:40 | ||||
| chr4:39458856-39459122 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527504-39527754 | Common:2; Rare:62 | ||||
| chr4:39638847-39639047 | Common:1; Rare:66 | ||||
| chr4:39697974-39698192 | Common:1; Rare:86 | ||||
| chr4:40056689-40056930 | Common:4; Rare:83 | ||||
| chr4:41990401-41990573 | Common:1; Rare:63 | ||||
| chr4:44678369-44678706 | Common:1; Rare:125 | ||||
| chr4:47463647-47463790 | Common:2; Rare:45 | ||||
| chr4:55125575-55125694 | Common:2; Rare:25 | ||||
| chr4:55546816-55546992 | Common:2; Rare:61 | ||||
| chr4:56387428-56387547 | Rare:43 | ||||
| chr4:56435439-56435973 | Common:6; Rare:172 | ||||
| chr4:56435998-56436307 | Rare:108 | ||||
| chr4:56467542-56467641 | Rare:38 |