| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45038965-45039094 | Rare:43 | ||||
| chr19:45370548-45370731 | Common:2; Rare:53 | ||||
| chr19:45405012-45405224 | Common:1; Rare:45 | ||||
| chr19:45406346-45406687 | Common:2; Rare:86 | ||||
| chr19:45423421-45423821 | Common:4; Rare:86; Clinvar (benign):2 | ||||
| chr19:45423832-45423859 | Rare:6 | ||||
| chr19:45423892-45423939 | Common:1; Rare:9 | ||||
| chr19:45450733-45451041 | Common:4; Rare:58 | ||||
| chr19:45507228-45507517 | Common:1; Rare:75 | ||||
| chr19:45584774-45585036 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45730869-45731067 | Common:1; Rare:43 | ||||
| chr19:46346938-46347139 | Common:3; Rare:64 | ||||
| chr19:46413521-46413773 | Common:1; Rare:83 | ||||
| chr19:46600895-46601420 | Common:5; Rare:182; Clinvar (benign):1 | ||||
| chr19:46787283-46787547 | Common:1; Rare:76 |