| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36252795-36253195 | Rare:168 | ||||
| chr22:36253200-36253443 | Rare:104 | ||||
| chr22:36328642-36329105 | Rare:161 | ||||
| chr22:36329250-36329650 | Common:1; Rare:126 | ||||
| chr22:36365010-36365462 | Common:3; Rare:158 | ||||
| chr22:36387921-36388478 | Common:32; Rare:907; Clinvar:8; Clinvar (benign):6 | ||||
| chr22:36480372-36481346 | Common:1; Rare:332; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr22:36481290-36481850 | Common:19; Rare:488 | ||||
| chr22:36481890-36482350 | Common:14; Rare:614 | ||||
| chr22:36506771-36506875 | Common:1; Rare:16 | ||||
| chr22:36506784-36507294 | Common:31; Rare:743 | ||||
| chr22:36528860-36529677 | Common:38; Rare:1023 | ||||
| chr22:36529679-36530246 | Common:6; Rare:183 | ||||
| chr22:36776001-36776612 | Common:16; Rare:477 | ||||
| chr22:36860770-36861172 | Common:4; Rare:134; Clinvar (benign):2 |