| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46053789-46053869 | Rare:30 | ||||
| chr22:46250268-46250387 | Common:1; Rare:34 | ||||
| chr22:46762509-46762728 | Common:3; Rare:76 | ||||
| chr22:49918412-49918694 | Common:1; Rare:103 | ||||
| chr22:50190418-50190674 | Common:3; Rare:81 | ||||
| chr22:50192522-50192624 | Common:1; Rare:21 | ||||
| chr22:50278136-50278535 | Rare:123 | ||||
| chr22:50526844-50527258 | Common:1; Rare:137; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:50530949-50531265 | Common:1; Rare:104 | ||||
| chr22:50531665-50531847 | Common:2; Rare:36 | ||||
| chr22:50532122-50532257 | Rare:33 | ||||
| chr22:50532444-50532685 | Common:2; Rare:55 | ||||
| chr22:50582365-50582575 | Common:1; Rare:105; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:50582752-50583124 | Common:7; Rare:120; Clinvar:2; Clinvar (benign):4 | ||||
| chr22:50783598-50783821 | Common:2; Rare:73 |