| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38243989-38244042 | Common:1; Rare:12 | ||||
| chr19:38256139-38256684 | Common:5; Rare:122 | ||||
| chr19:38263781-38264112 | Common:2; Rare:49 | ||||
| chr19:38264379-38264987 | Common:2; Rare:169 | ||||
| chr19:38290121-38290575 | Common:1; Rare:120; Clinvar (pathogenic):1 | ||||
| chr19:38315883-38316277 | Common:2; Rare:110 | ||||
| chr19:38319630-38319865 | Common:2; Rare:55 | ||||
| chr19:38374673-38374988 | Common:1; Rare:118 | ||||
| chr19:38391450-38391531 | Rare:14 | ||||
| chr19:38402929-38403259 | Common:6; Rare:111 | ||||
| chr19:38618912-38619323 | Common:3; Rare:115 | ||||
| chr19:38647504-38647772 | Common:2; Rare:96 | ||||
| chr19:38647872-38648543 | Common:5; Rare:136 | ||||
| chr19:38648545-38649423 | Common:6; Rare:138 | ||||
| chr19:38723612-38724075 | Common:1; Rare:126; Clinvar (benign):2 |