| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7939697-7940014 | Common:1; Rare:132 | ||||
| chr4:8440692-8440809 | Rare:47 | ||||
| chr4:10019014-10019127 | Rare:41; Clinvar (benign):1 | ||||
| chr4:10457324-10457446 | Common:4; Rare:48 | ||||
| chr4:11428842-11429052 | Common:2; Rare:60 | ||||
| chr4:13627717-13627877 | Common:1; Rare:47 | ||||
| chr4:15002225-15002505 | Common:2; Rare:109 | ||||
| chr4:15469679-15469896 | Common:1; Rare:45 | ||||
| chr4:15655289-15655491 | Common:1; Rare:91 | ||||
| chr4:15681553-15681869 | Common:3; Rare:110 | ||||
| chr4:16083678-16084032 | Common:4; Rare:104 | ||||
| chr4:16898509-16898884 | Common:14; Rare:69 | ||||
| chr4:17512064-17512185 | Common:3; Rare:56; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:17577327-17577544 | Rare:103 | ||||
| chr4:17614548-17614651 | Common:2; Rare:44 |