| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219279002-219279539 | Common:3; Rare:150; Clinvar (benign):1 | ||||
| chr2:219498691-219498943 | Common:2; Rare:57 | ||||
| chr2:219543724-219544056 | Common:3; Rare:101 | ||||
| chr2:219597684-219597888 | Common:1; Rare:73 | ||||
| chr2:221572301-221572447 | Common:2; Rare:47 | ||||
| chr2:222656014-222656453 | Common:3; Rare:148 | ||||
| chr2:223945152-223945439 | Rare:115 | ||||
| chr2:223957351-223957651 | Common:1; Rare:121; Clinvar (benign):2 | ||||
| chr2:224039271-224039375 | Rare:40 | ||||
| chr2:224585007-224585155 | Rare:65 | ||||
| chr2:226794795-226795131 | Common:1; Rare:90 | ||||
| chr2:226799545-226799834 | Rare:75 | ||||
| chr2:226799836-226800165 | Common:1; Rare:90 | ||||
| chr2:226835883-226836096 | Rare:86 | ||||
| chr2:226836355-226836394 | Common:1; Rare:8 |