| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40443020-40443530 | Common:6; Rare:204 | ||||
| chr19:40444263-40444522 | Common:6; Rare:135 | ||||
| chr19:40444600-40444920 | Common:3; Rare:194 | ||||
| chr19:40465705-40466113 | Common:5; Rare:218 | ||||
| chr19:40576678-40576905 | Common:3; Rare:65 | ||||
| chr19:40597036-40597288 | Rare:150 | ||||
| chr19:40606127-40606430 | Common:2; Rare:89; Clinvar (benign):4 | ||||
| chr19:40609790-40610265 | Common:11; Rare:186; Clinvar (benign):1 | ||||
| chr19:40690573-40690935 | Common:6; Rare:136 | ||||
| chr19:40714936-40715213 | Rare:125 | ||||
| chr19:40715620-40716040 | Common:7; Rare:144 | ||||
| chr19:40716060-40716380 | Common:3; Rare:47 | ||||
| chr19:40716853-40717174 | Common:2; Rare:207 | ||||
| chr19:40717219-40717357 | Common:1; Rare:45 | ||||
| chr19:40750397-40750606 | Common:7; Rare:117 |