| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6393361-6393591 | Common:2; Rare:69 | ||||
| chr19:6740619-6740939 | Common:1; Rare:74 | ||||
| chr19:7069663-7069731 | Common:1; Rare:20 | ||||
| chr19:7395025-7395195 | Common:4; Rare:53 | ||||
| chr19:7488995-7489078 | Rare:38 | ||||
| chr19:7534103-7534187 | Common:3; Rare:22; Clinvar (benign):1 | ||||
| chr19:7535574-7535785 | Common:3; Rare:77 | ||||
| chr19:7629529-7629842 | Common:5; Rare:112; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7943638-7943988 | Rare:94 | ||||
| chr19:8005498-8005822 | Common:1; Rare:114 | ||||
| chr19:8308288-8308638 | Common:3; Rare:113; Clinvar (benign):1 | ||||
| chr19:8321308-8321703 | Common:2; Rare:159 | ||||
| chr19:8364030-8364162 | Common:1; Rare:36 | ||||
| chr19:8390036-8390411 | Common:1; Rare:105 | ||||
| chr19:8444744-8445110 | Common:4; Rare:163; Clinvar (benign):1 |