| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17555460-17555723 | Common:1; Rare:71 | ||||
| chr19:17556086-17556486 | Common:1; Rare:106 | ||||
| chr19:17719327-17719520 | Common:2; Rare:69 | ||||
| chr19:17762750-17763030 | Rare:79 | ||||
| chr19:17841920-17842340 | Common:4; Rare:100; Clinvar:1 | ||||
| chr19:17847401-17847901 | Common:8; Rare:323 | ||||
| chr19:17859560-17859960 | Common:3; Rare:115 | ||||
| chr19:17932933-17933068 | Common:2; Rare:44 | ||||
| chr19:17952007-17952309 | Common:3; Rare:85 | ||||
| chr19:17966933-17967134 | Rare:54 | ||||
| chr19:18152488-18152655 | Rare:42 | ||||
| chr19:18152900-18153274 | Common:1; Rare:114 | ||||
| chr19:18161360-18161620 | Common:2; Rare:68; Clinvar (benign):2 | ||||
| chr19:18192601-18193508 | Common:10; Rare:451; Clinvar:2 | ||||
| chr19:18232730-18233250 | Rare:138 |