| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40444044-40444145 | Rare:22 | ||||
| chr19:40444182-40444633 | Common:4; Rare:132 | ||||
| chr19:40444639-40444953 | Common:2; Rare:104 | ||||
| chr19:40445068-40445115 | Rare:6 | ||||
| chr19:40465514-40466011 | Common:2; Rare:182 | ||||
| chr19:40530522-40530550 | Rare:7 | ||||
| chr19:40570487-40570776 | Common:2; Rare:93; Clinvar (pathogenic):1 | ||||
| chr19:40576708-40576941 | Common:3; Rare:79 | ||||
| chr19:40577384-40577429 | Rare:9 | ||||
| chr19:40596988-40597211 | Rare:67 | ||||
| chr19:40601204-40601390 | Rare:57 | ||||
| chr19:40606271-40606424 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr19:40609614-40609759 | Common:1; Rare:46 | ||||
| chr19:40609903-40610002 | Common:1; Rare:17 | ||||
| chr19:40610005-40610050 | Common:1; Rare:9 |