| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:98608332-98608840 | Common:6; Rare:423; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:98609089-98609882 | Common:6; Rare:243 | ||||
| chr2:98730081-98730816 | Common:5; Rare:293 | ||||
| chr2:98730848-98731439 | Common:15; Rare:394 | ||||
| chr2:98869230-98869609 | Common:7; Rare:186 | ||||
| chr2:98869770-98870270 | Common:6; Rare:131 | ||||
| chr2:98935853-98936514 | Common:5; Rare:278 | ||||
| chr2:99141022-99141829 | Common:9; Rare:757 | ||||
| chr2:99154760-99155210 | Common:17; Rare:398; Clinvar (benign):9 | ||||
| chr2:99155325-99155653 | Common:2; Rare:76 | ||||
| chr2:99180855-99181320 | Common:6; Rare:308 | ||||
| chr2:99181280-99181520 | Rare:94 | ||||
| chr2:99336214-99336648 | Common:2; Rare:122 | ||||
| chr2:99337175-99337532 | Rare:289 | ||||
| chr2:99489880-99490415 | Common:5; Rare:455 |