| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35257332-35257580 | Common:3; Rare:161 | ||||
| chr22:35257610-35258051 | Common:2; Rare:237 | ||||
| chr22:35299695-35299947 | Common:3; Rare:106 | ||||
| chr22:35300000-35300400 | Common:9; Rare:282 | ||||
| chr22:35380720-35381182 | Common:22; Rare:320 | ||||
| chr22:35399874-35400252 | Rare:364 | ||||
| chr22:35540234-35540560 | Common:4; Rare:186 | ||||
| chr22:35622352-35622945 | Common:11; Rare:239 | ||||
| chr22:35840368-35840478 | Rare:20 | ||||
| chr22:36028419-36029113 | Common:9; Rare:410 | ||||
| chr22:36204741-36204983 | Common:5; Rare:50 | ||||
| chr22:36239505-36239760 | Common:2; Rare:121 | ||||
| chr22:36328373-36328578 | Common:1; Rare:34 | ||||
| chr22:36387265-36387665 | Common:4; Rare:139 | ||||
| chr22:36387800-36388679 | Common:18; Rare:488; Clinvar:4; Clinvar (benign):2 |