| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241735434-241735528 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:241858842-241859080 | Common:1; Rare:57 | ||||
| chr20:290372-290622 | Common:13; Rare:67 | ||||
| chr20:291195-291290 | Rare:17 | ||||
| chr20:297222-297679 | Common:6; Rare:139 | ||||
| chr20:325196-325432 | Rare:62 | ||||
| chr20:325773-325882 | Rare:27 | ||||
| chr20:346950-347190 | Common:1; Rare:70 | ||||
| chr20:347631-348016 | Common:2; Rare:99 | ||||
| chr20:348131-348311 | Common:1; Rare:47 | ||||
| chr20:348485-348718 | Common:1; Rare:55 | ||||
| chr20:380754-381074 | Common:2; Rare:82 | ||||
| chr20:381783-382132 | Common:16; Rare:84 | ||||
| chr20:407721-408176 | Common:24; Rare:104 | ||||
| chr20:408190-408510 | Common:1; Rare:75 |