| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40465650-40466008 | Common:2; Rare:121 | ||||
| chr19:40609839-40610246 | Common:5; Rare:89 | ||||
| chr19:40610967-40611237 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:40623477-40623608 | Rare:32 | ||||
| chr19:40715059-40715187 | Rare:34 | ||||
| chr19:40716876-40717112 | Common:1; Rare:73 | ||||
| chr19:40717155-40717400 | Common:1; Rare:82 | ||||
| chr19:40717649-40718032 | Rare:112 | ||||
| chr19:40750426-40750618 | Common:5; Rare:59 | ||||
| chr19:40750803-40750922 | Common:1; Rare:22 | ||||
| chr19:40751076-40751477 | Common:3; Rare:125 | ||||
| chr19:40777921-40778298 | Common:1; Rare:103 | ||||
| chr19:41262326-41262566 | Rare:45 | ||||
| chr19:41264982-41265109 | Common:2; Rare:26 | ||||
| chr19:41310133-41310272 | Rare:56 |