| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6361763-6361897 | Rare:58; Clinvar (benign):1 | ||||
| chr19:6393385-6393739 | Common:5; Rare:106 | ||||
| chr19:6740665-6740939 | Common:1; Rare:62 | ||||
| chr19:7395032-7395185 | Common:4; Rare:47 | ||||
| chr19:7489006-7489115 | Rare:50 | ||||
| chr19:7533916-7534205 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chr19:7535574-7535745 | Common:3; Rare:57 | ||||
| chr19:7629502-7629848 | Common:7; Rare:128; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637003-7637143 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr19:7920201-7920364 | Rare:65 | ||||
| chr19:7943627-7944000 | Rare:105 | ||||
| chr19:8005498-8005829 | Common:1; Rare:118 | ||||
| chr19:8308296-8308647 | Common:2; Rare:110 | ||||
| chr19:8321308-8321714 | Common:2; Rare:163 | ||||
| chr19:8343254-8343418 | Rare:38 |