| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49959010-49959440 | Common:1; Rare:157 | ||||
| chr22:49970710-49971190 | Common:5; Rare:152 | ||||
| chr22:49971190-49971680 | Common:5; Rare:165 | ||||
| chr22:50293959-50294212 | Common:4; Rare:73 | ||||
| chr22:50308632-50308854 | Common:3; Rare:46 | ||||
| chr22:50387391-50387722 | Common:1; Rare:111 | ||||
| chr22:50396770-50397390 | Common:9; Rare:238 | ||||
| chr22:50406310-50406690 | Common:1; Rare:58 | ||||
| chr22:50627270-50627590 | Common:2; Rare:268; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):19 | ||||
| chr22:50641850-50642260 | Rare:120 | ||||
| chr22:50700270-50700650 | Common:1; Rare:117 | ||||
| chr3:9467360-9467610 | Common:1; Rare:38 | ||||
| chr3:9897810-9898240 | Common:6; Rare:153 | ||||
| chr3:9914930-9915340 | Common:4; Rare:139 | ||||
| chr3:10319720-10320030 | Common:9; Rare:68 |