| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45079151-45079363 | Rare:58 | ||||
| chr19:45079660-45079781 | Rare:41 | ||||
| chr19:45092827-45093220 | Common:3; Rare:117 | ||||
| chr19:45178204-45178557 | Common:4; Rare:103 | ||||
| chr19:45370524-45370803 | Common:2; Rare:86; Clinvar:1 | ||||
| chr19:45406331-45406724 | Common:3; Rare:98 | ||||
| chr19:45423491-45423670 | Common:2; Rare:38; Clinvar (benign):1 | ||||
| chr19:45423831-45423975 | Common:2; Rare:31 | ||||
| chr19:45424342-45424534 | Common:3; Rare:20 | ||||
| chr19:45450751-45451031 | Common:4; Rare:51 | ||||
| chr19:45468307-45468497 | Rare:44 | ||||
| chr19:45496957-45497271 | Common:2; Rare:96 | ||||
| chr19:45506819-45506949 | Common:1; Rare:41 | ||||
| chr19:45507387-45507533 | Rare:47 | ||||
| chr19:45640383-45640605 | Common:8; Rare:40 |