| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:29205745-29206155 | Common:2; Rare:96 | ||||
| chr22:29267026-29267301 | Common:1; Rare:67 | ||||
| chr22:29267694-29267767 | Common:1; Rare:25 | ||||
| chr22:29267808-29268367 | Common:2; Rare:166 | ||||
| chr22:29268609-29268753 | Rare:66 | ||||
| chr22:29388462-29388761 | Rare:92 | ||||
| chr22:29553233-29553379 | Rare:27 | ||||
| chr22:29553638-29553903 | Common:3; Rare:96 | ||||
| chr22:29581024-29581302 | Common:3; Rare:84 | ||||
| chr22:29603143-29603747 | Common:5; Rare:139; Clinvar:3 | ||||
| chr22:29603775-29603822 | Common:1; Rare:8; Clinvar (benign):1 | ||||
| chr22:29603981-29604092 | Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:29604112-29604199 | Rare:22; Clinvar (benign):1 | ||||
| chr22:29766195-29766495 | Common:1; Rare:51 | ||||
| chr22:29766803-29767011 | Common:1; Rare:56 |