| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12806744-12807144 | Common:4; Rare:228; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr19:12833585-12833985 | Rare:265 | ||||
| chr19:12834008-12834408 | Rare:102 | ||||
| chr19:12835290-12835706 | Common:6; Rare:221 | ||||
| chr19:12837605-12839215 | Common:13; Rare:756 | ||||
| chr19:12840540-12840971 | Rare:307 | ||||
| chr19:12847610-12847900 | Common:2; Rare:92 | ||||
| chr19:12878501-12879151 | Common:2; Rare:290 | ||||
| chr19:12881369-12881769 | Common:1; Rare:312 | ||||
| chr19:12886392-12887201 | Common:2; Rare:200; Clinvar:1 | ||||
| chr19:12887103-12887526 | Common:5; Rare:201; Clinvar:2 | ||||
| chr19:12887560-12887710 | Common:1; Rare:35 | ||||
| chr19:12890752-12891291 | Common:7; Rare:496; Clinvar:8; Clinvar (benign):8 | ||||
| chr19:12919164-12919564 | Common:10; Rare:696 | ||||
| chr19:12932896-12933333 | Common:1; Rare:147 |