| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10928521-10928888 | Common:4; Rare:228 | ||||
| chr19:10960647-10961167 | Common:12; Rare:390; Clinvar (benign):4 | ||||
| chr19:10983945-10984339 | Rare:192; Clinvar:39; Clinvar (benign):23 | ||||
| chr19:11089295-11089580 | Rare:116; Clinvar:26; Clinvar (pathogenic):7 | ||||
| chr19:11090320-11090670 | Common:4; Rare:195 | ||||
| chr19:11155768-11156059 | Common:3; Rare:68 | ||||
| chr19:11197517-11197684 | Common:1; Rare:55 | ||||
| chr19:11236569-11237350 | Common:15; Rare:322; Clinvar:2 | ||||
| chr19:11239490-11239634 | Common:4; Rare:75 | ||||
| chr19:11262311-11262901 | Common:3; Rare:182 | ||||
| chr19:11374875-11375248 | Common:2; Rare:243 | ||||
| chr19:11435348-11435813 | Common:10; Rare:247; Clinvar:4; Clinvar (benign):9 | ||||
| chr19:11442202-11442602 | Common:4; Rare:193; Clinvar (benign):4 | ||||
| chr19:11529050-11529327 | Common:1; Rare:99 | ||||
| chr19:11559188-11559468 | Common:7; Rare:165 |