| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:89111347-89111631 | Common:4; Rare:103 | ||||
| chr4:94451760-94452002 | Common:3; Rare:83 | ||||
| chr4:98261153-98261510 | Common:1; Rare:113 | ||||
| chr4:98658609-98658919 | Common:2; Rare:84 | ||||
| chr4:98929093-98929385 | Common:3; Rare:74 | ||||
| chr4:98995515-98995783 | Common:5; Rare:88 | ||||
| chr4:99088696-99088891 | Common:6; Rare:90 | ||||
| chr4:99563931-99564140 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99950248-99950485 | Rare:48 | ||||
| chr4:101347576-101347870 | Common:4; Rare:82 | ||||
| chr4:102501366-102501682 | Rare:88 | ||||
| chr4:102760934-102761084 | Rare:49; Clinvar:1 | ||||
| chr4:102826650-102826992 | Common:1; Rare:96 | ||||
| chr4:102827053-102827610 | Common:3; Rare:211 | ||||
| chr4:102827625-102827902 | Common:4; Rare:89 |