| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99894347-99894613 | Common:2; Rare:94 | ||||
| chr4:99950213-99950535 | Common:1; Rare:82 | ||||
| chr4:100190444-100190572 | Common:2; Rare:33 | ||||
| chr4:102345473-102345618 | Rare:36 | ||||
| chr4:102760903-102761084 | Rare:64; Clinvar:1 | ||||
| chr4:102826770-102826959 | Rare:54 | ||||
| chr4:102827442-102828299 | Common:7; Rare:284 | ||||
| chr4:102868850-102869114 | Common:2; Rare:94; Clinvar:1 | ||||
| chr4:105473958-105474181 | Common:5; Rare:109 | ||||
| chr4:105708641-105708874 | Common:3; Rare:77 | ||||
| chr4:106316173-106316601 | Common:5; Rare:136 | ||||
| chr4:107720166-107720538 | Common:7; Rare:153 | ||||
| chr4:107989686-107989907 | Common:5; Rare:104; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620719 | Common:6; Rare:145 | ||||
| chr4:109560068-109560379 | Common:5; Rare:91 |