| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143263371-143263537 | Rare:53 | ||||
| chr7:143288051-143288451 | Common:2; Rare:135 | ||||
| chr7:143380853-143381354 | Common:2; Rare:147 | ||||
| chr7:143620583-143620998 | Rare:15 | ||||
| chr7:143902089-143902304 | Common:7; Rare:70 | ||||
| chr7:144835972-144836122 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr7:148698513-148699010 | Common:5; Rare:174 | ||||
| chr7:148884197-148884480 | Common:1; Rare:131; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:149028322-149028391 | Rare:24 | ||||
| chr7:149028398-149029043 | Common:7; Rare:228 | ||||
| chr7:149090676-149090915 | Rare:64 | ||||
| chr7:149126214-149126449 | Common:6; Rare:80 | ||||
| chr7:149239474-149239672 | Rare:46 | ||||
| chr7:149460841-149461161 | Common:1; Rare:55 | ||||
| chr7:149714682-149715066 | Common:4; Rare:121 |