| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40601218-40601384 | Rare:53 | ||||
| chr19:40623472-40623695 | Rare:58; Clinvar:1 | ||||
| chr19:40714594-40714766 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr19:40715074-40715210 | Rare:37 | ||||
| chr19:40715748-40715912 | Common:3; Rare:27 | ||||
| chr19:40716076-40716283 | Common:2; Rare:31 | ||||
| chr19:40716848-40717114 | Common:1; Rare:89 | ||||
| chr19:40717156-40717404 | Common:1; Rare:84 | ||||
| chr19:40717836-40717917 | Rare:24 | ||||
| chr19:40718056-40718181 | Rare:43 | ||||
| chr19:40750426-40750767 | Common:5; Rare:90 | ||||
| chr19:40751033-40751283 | Common:3; Rare:80 | ||||
| chr19:40751758-40752042 | Common:1; Rare:64 | ||||
| chr19:40777934-40778280 | Common:1; Rare:97 | ||||
| chr19:41218678-41218992 | Common:8; Rare:68 |