| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215364878-215365243 | Common:3; Rare:81 | ||||
| chr2:215375212-215375725 | Common:2; Rare:138 | ||||
| chr2:215409635-215410110 | Rare:119 | ||||
| chr2:215435637-215435695 | Rare:18 | ||||
| chr2:215435705-215436287 | Common:4; Rare:158 | ||||
| chr2:216081748-216081925 | Common:1; Rare:64 | ||||
| chr2:216412268-216412561 | Common:3; Rare:68; Clinvar (benign):2 | ||||
| chr2:216412665-216412788 | Rare:15 | ||||
| chr2:216498687-216499103 | Common:13; Rare:149 | ||||
| chr2:218217046-218217246 | Common:1; Rare:70 | ||||
| chr2:218269701-218269905 | Rare:44 | ||||
| chr2:218270062-218270601 | Common:5; Rare:174; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:218287255-218287427 | Common:1; Rare:29 | ||||
| chr2:218322988-218323307 | Common:6; Rare:105 | ||||
| chr2:218398099-218398239 | Common:1; Rare:46 |