| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827670-102828142 | Common:3; Rare:147 | ||||
| chr4:102868850-102869068 | Common:2; Rare:77 | ||||
| chr4:105708644-105708843 | Common:1; Rare:64 | ||||
| chr4:106316060-106316159 | Rare:25 | ||||
| chr4:106316169-106316617 | Common:5; Rare:144 | ||||
| chr4:107720151-107720493 | Common:8; Rare:140 | ||||
| chr4:107989690-107989927 | Common:5; Rare:109; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620378-108620636 | Common:6; Rare:130 | ||||
| chr4:109433783-109433948 | Common:1; Rare:51 | ||||
| chr4:109815475-109815562 | Rare:30 | ||||
| chr4:112285898-112285953 | Rare:14 | ||||
| chr4:112636886-112637181 | Rare:81 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:113761113-113761254 | Common:1; Rare:34 | ||||
| chr4:118685270-118685541 | Common:3; Rare:81 |