| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69387183-69387384 | Rare:52; Clinvar:2 | ||||
| chr2:69437421-69437520 | Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:69643622-69643825 | Rare:73 | ||||
| chr2:69742012-69742152 | Rare:31 | ||||
| chr2:69829517-69829737 | Common:1; Rare:87 | ||||
| chr2:70086971-70087067 | Rare:47 | ||||
| chr2:70087372-70087750 | Common:2; Rare:147 | ||||
| chr2:70190986-70191124 | Rare:33 | ||||
| chr2:70257902-70258167 | Common:1; Rare:83 | ||||
| chr2:70293381-70293470 | Rare:29 | ||||
| chr2:70293645-70294048 | Common:4; Rare:110 | ||||
| chr2:70553806-70554240 | Common:3; Rare:127 | ||||
| chr2:71068534-71068678 | Rare:66 | ||||
| chr2:71130218-71130698 | Common:7; Rare:140; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276450-71276651 | Rare:75 |