| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37658340-37658773 | Common:8; Rare:218 | ||||
| chr22:37675375-37675681 | Common:3; Rare:91 | ||||
| chr22:37686255-37686400 | Common:1; Rare:55 | ||||
| chr22:37745942-37746316 | Common:8; Rare:255; Clinvar (benign):2 | ||||
| chr22:37805290-37805837 | Rare:235 | ||||
| chr22:37807626-37808033 | Common:8; Rare:220 | ||||
| chr22:37844266-37844590 | Common:4; Rare:171 | ||||
| chr22:37849285-37849483 | Rare:228 | ||||
| chr22:37906075-37906363 | Common:1; Rare:76 | ||||
| chr22:37953587-37953836 | Rare:173 | ||||
| chr22:38057179-38057494 | Common:3; Rare:82 | ||||
| chr22:38110686-38110799 | Common:1; Rare:33 | ||||
| chr22:38110790-38111230 | Common:7; Rare:209 | ||||
| chr22:38143336-38143572 | Common:4; Rare:81 | ||||
| chr22:38180750-38181200 | Common:6; Rare:179 |