| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6393379-6393769 | Common:5; Rare:115 | ||||
| chr19:6416793-6417086 | Common:1; Rare:99 | ||||
| chr19:6424499-6424754 | Common:2; Rare:68 | ||||
| chr19:6710772-6711065 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6740605-6741104 | Common:1; Rare:128 | ||||
| chr19:7294412-7294544 | Common:1; Rare:36 | ||||
| chr19:7395014-7395218 | Common:6; Rare:61 | ||||
| chr19:7488976-7489051 | Rare:38 | ||||
| chr19:7535574-7535818 | Common:3; Rare:90 | ||||
| chr19:7539970-7540208 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr19:7629514-7629853 | Common:5; Rare:124; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636969-7637179 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr19:7641833-7642118 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7851494-7851710 | Common:1; Rare:45 | ||||
| chr19:7910771-7911143 | Common:2; Rare:145 |