| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:134918588-134918870 | Common:1; Rare:115 | ||||
| chr2:135052189-135052310 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr2:135530708-135530988 | Common:3; Rare:67 | ||||
| chr2:135531167-135531514 | Common:1; Rare:74 | ||||
| chr2:135984881-135985199 | Common:1; Rare:73 | ||||
| chr2:135985391-135985678 | Common:4; Rare:125; Clinvar (benign):1 | ||||
| chr2:135985687-135985803 | Common:1; Rare:37 | ||||
| chr2:137964355-137964565 | Common:1; Rare:43 | ||||
| chr2:138501645-138502037 | Common:4; Rare:144 | ||||
| chr2:138780282-138780494 | Rare:56 | ||||
| chr2:142130958-142131001 | Rare:10 | ||||
| chr2:144517460-144517643 | Common:5; Rare:45 | ||||
| chr2:144518386-144518532 | Rare:31 | ||||
| chr2:144520323-144520537 | Common:4; Rare:37; Clinvar (benign):1 | ||||
| chr2:144524431-144524627 | Common:4; Rare:51 |