| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47324530-47324740 | Common:3; Rare:40 | ||||
| chr19:47730216-47730399 | Common:1; Rare:27 | ||||
| chr19:48966271-48966745 | Common:1; Rare:164; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:49638292-49638362 | Rare:8 | ||||
| chr19:51693596-51693906 | Rare:71 | ||||
| chr2:3513863-3514094 | Common:3; Rare:60 | ||||
| chr2:9517902-9518208 | Rare:63 | ||||
| chr2:9523982-9524309 | Common:2; Rare:51 | ||||
| chr2:12715853-12716088 | Common:2; Rare:47 | ||||
| chr2:19348006-19348258 | Common:1; Rare:80 | ||||
| chr2:20448387-20449048 | Common:3; Rare:170 | ||||
| chr2:20450936-20450999 | Rare:18 | ||||
| chr2:24303797-24304156 | Rare:70 | ||||
| chr2:27070691-27071013 | Rare:62 | ||||
| chr2:27725491-27725552 | Rare:7 |