| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4831655-4832044 | Common:4; Rare:83 | ||||
| chr19:4867618-4867812 | Common:3; Rare:60 | ||||
| chr19:5622737-5623181 | Common:5; Rare:171 | ||||
| chr19:5978078-5978383 | Common:3; Rare:113 | ||||
| chr19:6110523-6110809 | Common:2; Rare:85 | ||||
| chr19:7394991-7395185 | Common:6; Rare:60 | ||||
| chr19:7489006-7489044 | Rare:18 | ||||
| chr19:7535574-7535747 | Common:3; Rare:57 | ||||
| chr19:7629523-7629848 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637043-7637143 | Common:2; Rare:36; Clinvar (benign):1 | ||||
| chr19:8005520-8005822 | Common:1; Rare:106 | ||||
| chr19:8321308-8321568 | Common:2; Rare:119 | ||||
| chr19:8364014-8364162 | Common:1; Rare:38 | ||||
| chr19:8390056-8390412 | Common:1; Rare:99 | ||||
| chr19:8514149-8514244 | Common:1; Rare:23 |