| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44500494-44500816 | Common:8; Rare:98 | ||||
| chr19:44643801-44643944 | Rare:38 | ||||
| chr19:45405019-45405163 | Rare:30 | ||||
| chr19:45406290-45406649 | Common:1; Rare:77 | ||||
| chr19:45423477-45423821 | Common:3; Rare:71; Clinvar (benign):1 | ||||
| chr19:45423831-45423945 | Common:2; Rare:30 | ||||
| chr19:45450733-45451067 | Common:4; Rare:64 | ||||
| chr19:45507366-45507528 | Rare:51 | ||||
| chr19:45584776-45585051 | Common:4; Rare:103; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45691898-45692098 | Rare:71 | ||||
| chr19:45692523-45692713 | Rare:46 | ||||
| chr19:45692916-45693007 | Rare:15 | ||||
| chr19:45769185-45769568 | Common:1; Rare:160 | ||||
| chr19:46148194-46148274 | Rare:18 | ||||
| chr19:46600978-46601409 | Common:4; Rare:147; Clinvar (benign):1 |