| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135741716-135741979 | Common:1; Rare:100 | ||||
| chr2:135985423-135985672 | Common:4; Rare:113; Clinvar (benign):1 | ||||
| chr2:142130730-142130811 | Common:2; Rare:35 | ||||
| chr2:142130813-142131053 | Rare:65 | ||||
| chr2:142131374-142131429 | Rare:12 | ||||
| chr2:144332453-144332672 | Rare:87 | ||||
| chr2:144518394-144518495 | Rare:25 | ||||
| chr2:147844932-147845081 | Common:4; Rare:18 | ||||
| chr2:147845287-147845412 | Common:1; Rare:24 | ||||
| chr2:148020656-148021307 | Common:2; Rare:156; Clinvar (benign):2 | ||||
| chr2:148021332-148021721 | Rare:99; Clinvar (benign):1 | ||||
| chr2:148644520-148644764 | Rare:76 | ||||
| chr2:148875105-148875232 | Common:1; Rare:27 | ||||
| chr2:148875550-148875711 | Common:2; Rare:49; Clinvar (benign):3 | ||||
| chr2:149587131-149587320 | Common:3; Rare:40; Clinvar:1; Clinvar (benign):1 |