| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95277564-95277962 | Common:1; Rare:79 | ||||
| chr2:95346270-95346650 | Common:2; Rare:258 | ||||
| chr2:95402512-95402824 | Rare:211 | ||||
| chr2:95991582-95991757 | Rare:50 | ||||
| chr2:96116460-96116807 | Common:6; Rare:206 | ||||
| chr2:96138390-96138890 | Common:7; Rare:214 | ||||
| chr2:96144394-96144684 | Common:1; Rare:73 | ||||
| chr2:96144930-96145390 | Rare:212 | ||||
| chr2:96145316-96145645 | Common:5; Rare:168 | ||||
| chr2:96208224-96208501 | Rare:356 | ||||
| chr2:96208560-96208720 | Common:3; Rare:45 | ||||
| chr2:96208663-96209146 | Common:13; Rare:378 | ||||
| chr2:96265886-96266379 | Common:6; Rare:401; Clinvar:8 | ||||
| chr2:96305385-96305755 | Common:8; Rare:305; Clinvar:9; Clinvar (benign):6 | ||||
| chr2:96335652-96336190 | Common:9; Rare:349 |