| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7488997-7489051 | Rare:26 | ||||
| chr19:7535574-7535791 | Common:3; Rare:79 | ||||
| chr19:7629505-7629859 | Common:6; Rare:129; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636997-7637161 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7642104-7642333 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:7903505-7903929 | Common:2; Rare:141 | ||||
| chr19:7920236-7920393 | Rare:73 | ||||
| chr19:7943621-7943990 | Rare:104 | ||||
| chr19:8005498-8005822 | Common:1; Rare:114 | ||||
| chr19:8308291-8308639 | Common:2; Rare:112 | ||||
| chr19:8321308-8321703 | Common:2; Rare:159 | ||||
| chr19:8364012-8364167 | Common:1; Rare:41 | ||||
| chr19:8390032-8390449 | Common:2; Rare:116 | ||||
| chr19:8444805-8445110 | Common:2; Rare:139; Clinvar (benign):1 | ||||
| chr19:8526431-8526468 | Rare:11 |