| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219571398-219571892 | Common:1; Rare:95; Clinvar:3 | ||||
| chr2:219597677-219597911 | Common:2; Rare:165 | ||||
| chr2:219598059-219598256 | Common:2; Rare:119 | ||||
| chr2:222656054-222656570 | Common:4; Rare:216 | ||||
| chr2:222671456-222671718 | Common:3; Rare:122 | ||||
| chr2:222860720-222861164 | Common:6; Rare:249 | ||||
| chr2:222861380-222862020 | Common:4; Rare:196 | ||||
| chr2:223837557-223837677 | Common:1; Rare:30 | ||||
| chr2:223945274-223945493 | Common:1; Rare:85 | ||||
| chr2:223957248-223957508 | Common:8; Rare:184; Clinvar (benign):1 | ||||
| chr2:224585249-224585487 | Common:4; Rare:87 | ||||
| chr2:224585482-224585820 | Common:2; Rare:93 | ||||
| chr2:226799689-226800188 | Common:1; Rare:207 | ||||
| chr2:226836300-226836890 | Common:9; Rare:232 | ||||
| chr2:227325133-227325405 | Common:11; Rare:193 |