| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135876400-135876637 | Rare:64 | ||||
| chr2:135985413-135985895 | Common:5; Rare:174; Clinvar (benign):1 | ||||
| chr2:137964053-137964515 | Common:5; Rare:76 | ||||
| chr2:138501652-138502005 | Common:3; Rare:127 | ||||
| chr2:142877511-142877685 | Common:1; Rare:27 | ||||
| chr2:144517317-144517751 | Common:5; Rare:132; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144518363-144518525 | Rare:35 | ||||
| chr2:144520001-144520536 | Common:4; Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:148020681-148021115 | Common:2; Rare:100; Clinvar (benign):2 | ||||
| chr2:148021135-148021462 | Rare:73 | ||||
| chr2:148021552-148021658 | Rare:21 | ||||
| chr2:149587310-149587397 | Rare:16 | ||||
| chr2:149587685-149587838 | Common:1; Rare:44; Clinvar:1 | ||||
| chr2:151828439-151828793 | Common:2; Rare:100 |