| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40284808-40285250 | Common:4; Rare:311 | ||||
| chr19:40285187-40285900 | Common:21; Rare:973 | ||||
| chr19:40348254-40348797 | Common:29; Rare:922 | ||||
| chr19:40349086-40349486 | Common:1; Rare:70 | ||||
| chr19:40365371-40366101 | Common:18; Rare:502 | ||||
| chr19:40367016-40367166 | Common:2; Rare:33 | ||||
| chr19:40371610-40371736 | Common:2; Rare:32; Clinvar:1 | ||||
| chr19:40408272-40408672 | Common:2; Rare:158; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:40425300-40425770 | Common:14; Rare:320 | ||||
| chr19:40425760-40426269 | Common:22; Rare:546 | ||||
| chr19:40426297-40426697 | Common:3; Rare:98 | ||||
| chr19:40443005-40443518 | Common:15; Rare:355 | ||||
| chr19:40443452-40444230 | Common:7; Rare:290 | ||||
| chr19:40444212-40444612 | Common:21; Rare:560 | ||||
| chr19:40444589-40445036 | Common:9; Rare:503 |