| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4831655-4832044 | Common:4; Rare:83 | ||||
| chr19:4867617-4867814 | Common:3; Rare:60 | ||||
| chr19:5293211-5293433 | Common:1; Rare:99 | ||||
| chr19:5622746-5623181 | Common:5; Rare:164 | ||||
| chr19:5978078-5978384 | Common:3; Rare:114 | ||||
| chr19:7395037-7395179 | Common:4; Rare:45 | ||||
| chr19:7629520-7629842 | Common:5; Rare:116; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7943647-7943984 | Rare:85 | ||||
| chr19:8308312-8308638 | Common:2; Rare:99 | ||||
| chr19:8321308-8321694 | Common:2; Rare:157 | ||||
| chr19:8390038-8390390 | Common:1; Rare:96 | ||||
| chr19:8444702-8445040 | Common:4; Rare:142 | ||||
| chr19:9435554-9435617 | Rare:23 | ||||
| chr19:9538579-9538716 | Common:1; Rare:37 | ||||
| chr19:9621177-9621529 | Common:3; Rare:99 |