| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94451823-94451995 | Common:3; Rare:54 | ||||
| chr4:98261153-98261534 | Common:1; Rare:122 | ||||
| chr4:98929098-98929365 | Common:3; Rare:67 | ||||
| chr4:99088704-99088882 | Common:6; Rare:76 | ||||
| chr4:99894357-99894618 | Common:3; Rare:91 | ||||
| chr4:99950254-99950477 | Rare:43 | ||||
| chr4:101347558-101347834 | Common:4; Rare:83 | ||||
| chr4:101348060-101348190 | Rare:36 | ||||
| chr4:102826837-102827214 | Common:4; Rare:131 | ||||
| chr4:102827458-102828138 | Common:4; Rare:227 | ||||
| chr4:102868844-102869063 | Common:2; Rare:75 | ||||
| chr4:105708646-105708847 | Common:1; Rare:65 | ||||
| chr4:106316173-106316593 | Common:5; Rare:132 | ||||
| chr4:107824778-107825017 | Common:1; Rare:64 | ||||
| chr4:107989690-107989900 | Common:5; Rare:100; Clinvar:4; Clinvar (benign):5 |