| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6481738-6481859 | Common:1; Rare:32 | ||||
| chr19:6591137-6591210 | Rare:10 | ||||
| chr19:6604080-6604249 | Rare:23 | ||||
| chr19:6737247-6737331 | Rare:23 | ||||
| chr19:7348818-7349218 | Common:1; Rare:85 | ||||
| chr19:7534023-7534188 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr19:7535620-7535739 | Common:2; Rare:34 | ||||
| chr19:7629528-7629848 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636978-7637143 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr19:7943630-7944007 | Rare:109 | ||||
| chr19:8005504-8005835 | Common:1; Rare:118 | ||||
| chr19:8321308-8321703 | Common:2; Rare:159 | ||||
| chr19:8390044-8390411 | Common:1; Rare:105 | ||||
| chr19:8444802-8445045 | Common:2; Rare:114 | ||||
| chr19:8514148-8514256 | Common:1; Rare:27 |