| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44164923-44165175 | Common:2; Rare:62 | ||||
| chr19:44259811-44259971 | Common:1; Rare:56 | ||||
| chr19:44304975-44305164 | Rare:58 | ||||
| chr19:44356636-44356851 | Common:1; Rare:48 | ||||
| chr19:44643789-44643959 | Rare:51 | ||||
| chr19:44954903-44955028 | Common:2; Rare:36 | ||||
| chr19:44955247-44955463 | Common:2; Rare:71 | ||||
| chr19:45001890-45002204 | Common:6; Rare:76 | ||||
| chr19:45038967-45039104 | Rare:48 | ||||
| chr19:45068188-45068477 | Common:3; Rare:71 | ||||
| chr19:45069028-45069120 | Rare:31 | ||||
| chr19:45079173-45079380 | Rare:56 | ||||
| chr19:45091567-45091796 | Common:2; Rare:61 | ||||
| chr19:45092827-45093222 | Common:3; Rare:117 | ||||
| chr19:45178593-45178810 | Common:4; Rare:50; Clinvar:1; Clinvar (benign):3 |