| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38264249-38264676 | Common:6; Rare:106 | ||||
| chr19:38264791-38264904 | Rare:43 | ||||
| chr19:38315904-38316210 | Common:1; Rare:81 | ||||
| chr19:38374407-38374812 | Rare:149 | ||||
| chr19:38618926-38619310 | Common:3; Rare:111 | ||||
| chr19:38647372-38647785 | Common:3; Rare:138 | ||||
| chr19:38789026-38789204 | Common:4; Rare:31 | ||||
| chr19:38831753-38832061 | Common:4; Rare:93; Clinvar (benign):1 | ||||
| chr19:38899586-38900007 | Rare:122 | ||||
| chr19:38930724-38930992 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975724-38975884 | Common:1; Rare:41 | ||||
| chr19:39390981-39391425 | Common:1; Rare:170 | ||||
| chr19:39406710-39406873 | Rare:66 | ||||
| chr19:39407588-39407757 | Rare:40 | ||||
| chr19:39435866-39436188 | Common:8; Rare:126 |