| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46762506-46762701 | Common:3; Rare:70 | ||||
| chr22:49918402-49918710 | Common:1; Rare:117 | ||||
| chr22:50074704-50074943 | Common:1; Rare:56 | ||||
| chr22:50185725-50185993 | Common:5; Rare:106 | ||||
| chr22:50244632-50244662 | Rare:8 | ||||
| chr22:50244954-50245076 | Common:2; Rare:47 | ||||
| chr22:50282274-50282429 | Common:2; Rare:43 | ||||
| chr22:50466658-50466952 | Rare:93 | ||||
| chr22:50532124-50532210 | Rare:21 | ||||
| chr22:50562920-50563065 | Common:3; Rare:38 | ||||
| chr22:50582400-50582443 | Rare:22 | ||||
| chr22:50582784-50583142 | Common:7; Rare:119; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628046-50628276 | Common:9; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783585-50783859 | Common:2; Rare:91 | ||||
| chr3:197202-197296 | Rare:32 |