| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6393382-6393580 | Common:2; Rare:58 | ||||
| chr19:6737535-6737634 | Common:1; Rare:34 | ||||
| chr19:6740619-6740914 | Common:1; Rare:70 | ||||
| chr19:7395022-7395185 | Common:4; Rare:50 | ||||
| chr19:7489008-7489150 | Common:2; Rare:66 | ||||
| chr19:7535543-7535769 | Common:3; Rare:81; Clinvar:2 | ||||
| chr19:7629531-7629839 | Common:5; Rare:108; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7943644-7943988 | Rare:90 | ||||
| chr19:8005514-8005821 | Common:1; Rare:108 | ||||
| chr19:8308286-8308638 | Common:3; Rare:114; Clinvar (benign):1 | ||||
| chr19:8321308-8321567 | Common:2; Rare:119 | ||||
| chr19:8364022-8364162 | Common:1; Rare:36 | ||||
| chr19:8390038-8390411 | Common:1; Rare:105 | ||||
| chr19:8444836-8445008 | Common:2; Rare:72 | ||||
| chr19:9324140-9324319 | Common:3; Rare:95 |