| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40613238-40613457 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:40613533-40613596 | Rare:18 | ||||
| chr19:40613677-40614060 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:40614669-40614840 | Common:1; Rare:43 | ||||
| chr19:40690565-40690942 | Common:3; Rare:82 | ||||
| chr19:40691293-40691370 | Common:2; Rare:24 | ||||
| chr19:40715066-40715285 | Common:1; Rare:58 | ||||
| chr19:40715573-40715751 | Common:2; Rare:39 | ||||
| chr19:40716098-40716272 | Common:2; Rare:25 | ||||
| chr19:40716624-40717167 | Common:3; Rare:151 | ||||
| chr19:40717193-40717396 | Common:1; Rare:74 | ||||
| chr19:40750338-40750969 | Common:7; Rare:160 | ||||
| chr19:40750973-40751356 | Common:3; Rare:108 | ||||
| chr19:40751720-40751853 | Rare:32 | ||||
| chr19:40777825-40778475 | Common:1; Rare:163 |