| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41363794-41363983 | Common:1; Rare:69; Clinvar:1 | ||||
| chr19:41364128-41364180 | Rare:15 | ||||
| chr19:41397324-41397409 | Common:2; Rare:31 | ||||
| chr19:41397558-41397837 | Common:7; Rare:96; Clinvar (benign):4 | ||||
| chr19:41860038-41860466 | Common:5; Rare:162; Clinvar:4; Clinvar (benign):3 | ||||
| chr19:41884132-41884321 | Rare:41 | ||||
| chr19:41959284-41959459 | Common:1; Rare:57 | ||||
| chr19:42075756-42076215 | Common:5; Rare:135 | ||||
| chr19:42217671-42217874 | Rare:78 | ||||
| chr19:42220112-42220379 | Common:2; Rare:70 | ||||
| chr19:42243112-42243350 | Common:2; Rare:90 | ||||
| chr19:42255071-42255384 | Common:1; Rare:110 | ||||
| chr19:42268283-42268567 | Rare:59 | ||||
| chr19:42302247-42302689 | Rare:128 | ||||
| chr19:43527172-43527276 | Common:4; Rare:50; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):2 |