| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131105233-131105367 | Common:1; Rare:64 | ||||
| chr2:131492762-131493097 | Common:8; Rare:101 | ||||
| chr2:134918585-134918904 | Common:1; Rare:132 | ||||
| chr2:135052072-135052321 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr2:135052568-135052735 | Rare:35 | ||||
| chr2:135530548-135530661 | Rare:24 | ||||
| chr2:135531170-135531508 | Common:1; Rare:70 | ||||
| chr2:135741723-135741956 | Common:1; Rare:90 | ||||
| chr2:135985404-135985720 | Common:4; Rare:133; Clinvar (benign):1 | ||||
| chr2:138501645-138502005 | Common:4; Rare:133 | ||||
| chr2:142877511-142877724 | Common:2; Rare:32 | ||||
| chr2:144513785-144513954 | Rare:45 | ||||
| chr2:144517379-144517778 | Common:5; Rare:110; Clinvar (benign):2 | ||||
| chr2:144518134-144518143 | |||||
| chr2:144520302-144520526 | Common:4; Rare:42; Clinvar (benign):1 |