| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:212429180-212429368 | Rare:36 | ||||
| chr2:212538513-212538727 | Rare:70 | ||||
| chr2:213151585-213152013 | Common:1; Rare:175 | ||||
| chr2:213284232-213284500 | Rare:86 | ||||
| chr2:213923667-213923871 | Common:1; Rare:30 | ||||
| chr2:214809450-214809561 | Common:1; Rare:49; Clinvar:22; Clinvar (benign):13 | ||||
| chr2:214809620-214810239 | Common:11; Rare:208; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:215311933-215312348 | Common:9; Rare:173 | ||||
| chr2:215375360-215375630 | Common:1; Rare:66 | ||||
| chr2:215409727-215409847 | Rare:31 | ||||
| chr2:215436005-215436253 | Common:2; Rare:76 | ||||
| chr2:216081761-216081920 | Common:1; Rare:54 | ||||
| chr2:216112847-216113138 | Common:2; Rare:62 | ||||
| chr2:216412664-216412786 | Rare:14 | ||||
| chr2:216498753-216499405 | Common:13; Rare:198 |