| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178685236-178685404 | Common:3; Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:178688347-178688581 | Rare:34 | ||||
| chr2:178689487-178689823 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):8 | ||||
| chr2:178691833-178692164 | Rare:77; Clinvar:7; Clinvar (benign):5 | ||||
| chr2:178693572-178693724 | Common:1; Rare:39; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:178695840-178696554 | Common:1; Rare:145; Clinvar:18; Clinvar (benign):6 | ||||
| chr2:178697111-178697213 | Rare:13; Clinvar (benign):1 | ||||
| chr2:178704875-178705092 | Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:178706535-178707020 | Common:5; Rare:131; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr2:178711942-178712616 | Rare:200; Clinvar:24; Clinvar (benign):17 | ||||
| chr2:178713083-178713658 | Common:5; Rare:160; Clinvar:13; Clinvar (benign):15 | ||||
| chr2:178723039-178723703 | Rare:191; Clinvar:37; Clinvar (benign):12 | ||||
| chr2:178729657-178730357 | Common:2; Rare:187; Clinvar:14; Clinvar (benign):18 | ||||
| chr2:178731831-178732363 | Rare:140; Clinvar:14; Clinvar (benign):8 | ||||
| chr2:178769652-178770349 | Common:7; Rare:164; Clinvar:17; Clinvar (benign):19 |