| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215433582-215433833 | Common:1; Rare:54 | ||||
| chr2:217812126-217812446 | Common:3; Rare:62 | ||||
| chr2:217825053-217825369 | Common:1; Rare:60 | ||||
| chr2:217840820-217841073 | Common:2; Rare:38 | ||||
| chr2:217873404-217873483 | Rare:17 | ||||
| chr2:217878220-217878511 | Common:4; Rare:48 | ||||
| chr2:217898313-217898710 | Common:2; Rare:85 | ||||
| chr2:217906812-217907093 | Common:4; Rare:48 | ||||
| chr2:217980035-217980184 | Rare:23 | ||||
| chr2:218033955-218034075 | Rare:34 | ||||
| chr2:218272517-218272617 | Rare:36 | ||||
| chr2:218277081-218277147 | Common:1; Rare:20 | ||||
| chr2:218277364-218277737 | Rare:103 | ||||
| chr2:218313497-218313534 | Rare:5 | ||||
| chr2:218344515-218344833 | Common:1; Rare:96; Clinvar:3; Clinvar (benign):3 |