| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143843157-143843409 | Common:2; Rare:80 | ||||
| chr6:143843607-143844007 | Common:3; Rare:117 | ||||
| chr6:144006752-144007057 | Rare:65 | ||||
| chr6:144064032-144064234 | Common:1; Rare:40 | ||||
| chr6:144095533-144095872 | Common:6; Rare:90 | ||||
| chr6:144285115-144285494 | Common:3; Rare:104 | ||||
| chr6:144583217-144583502 | Rare:50 | ||||
| chr6:144659354-144659754 | Common:4; Rare:83 | ||||
| chr6:145734752-145735079 | Common:3; Rare:110 | ||||
| chr6:145735187-145735338 | Common:3; Rare:59; Clinvar:9; Clinvar (benign):4 | ||||
| chr6:145735496-145735681 | Common:3; Rare:54; Clinvar (benign):3 | ||||
| chr6:145735924-145736080 | Rare:25 | ||||
| chr6:145813838-145814513 | Rare:230 | ||||
| chr6:145814687-145814958 | Common:1; Rare:130 | ||||
| chr6:145815132-145815269 | Rare:27 |