| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43955303-43955566 | Common:3; Rare:80 | ||||
| chr22:44024117-44024364 | Common:2; Rare:77 | ||||
| chr22:44312826-44312965 | Rare:31 | ||||
| chr22:44752513-44752613 | Common:2; Rare:40 | ||||
| chr22:45163786-45164030 | Common:3; Rare:91 | ||||
| chr22:45309675-45309972 | Common:1; Rare:122 | ||||
| chr22:45413565-45413745 | Common:1; Rare:76 | ||||
| chr22:46053647-46053901 | Rare:87 | ||||
| chr22:46250268-46250396 | Common:1; Rare:39 | ||||
| chr22:46267865-46268037 | Common:1; Rare:54 | ||||
| chr22:46335601-46335767 | Common:2; Rare:72; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:46762506-46762693 | Common:3; Rare:68 | ||||
| chr22:50185741-50185942 | Common:4; Rare:89 | ||||
| chr22:50525531-50525685 | Common:4; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50562887-50563046 | Common:3; Rare:45 |