| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38872176-38872441 | Rare:71 | ||||
| chr22:38952534-38952788 | Rare:40 | ||||
| chr22:38957410-38957612 | Rare:39 | ||||
| chr22:39014080-39014298 | Common:1; Rare:53 | ||||
| chr22:39020806-39020923 | Common:1; Rare:33 | ||||
| chr22:39040575-39040879 | Common:1; Rare:55 | ||||
| chr22:39244958-39245262 | Common:1; Rare:64 | ||||
| chr22:39319500-39319791 | Common:5; Rare:136 | ||||
| chr22:39399670-39399805 | Common:3; Rare:57 | ||||
| chr22:39502131-39502436 | Rare:92 | ||||
| chr22:39521030-39521522 | Common:7; Rare:179 | ||||
| chr22:40044149-40044327 | Common:2; Rare:35 | ||||
| chr22:40044579-40044891 | Common:2; Rare:69 | ||||
| chr22:40346441-40346580 | Rare:62; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40370430-40370664 | Rare:89 |