| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44356635-44356818 | Common:1; Rare:36 | ||||
| chr19:44643793-44644032 | Rare:61 | ||||
| chr19:44808932-44809126 | Rare:65 | ||||
| chr19:44905571-44906070 | Common:4; Rare:131; Clinvar:1 | ||||
| chr19:44914543-44914949 | Common:1; Rare:108 | ||||
| chr19:44947061-44947215 | Common:3; Rare:33 | ||||
| chr19:44954949-44955028 | Common:2; Rare:26 | ||||
| chr19:44955251-44955410 | Common:2; Rare:45 | ||||
| chr19:45091585-45091794 | Common:1; Rare:55 | ||||
| chr19:45370548-45370765 | Common:2; Rare:66 | ||||
| chr19:45406350-45406685 | Common:2; Rare:84 | ||||
| chr19:45423502-45423821 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chr19:45423844-45423980 | Common:2; Rare:31 | ||||
| chr19:45507317-45507583 | Rare:81 | ||||
| chr19:45584765-45585056 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):4 |