| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35257397-35257513 | Common:1; Rare:30 | ||||
| chr22:35300057-35300320 | Common:1; Rare:85 | ||||
| chr22:35399904-35400197 | Rare:102 | ||||
| chr22:36387935-36388322 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481294-36481404 | Common:1; Rare:21 | ||||
| chr22:36481564-36481747 | Common:2; Rare:49 | ||||
| chr22:36529074-36529531 | Common:6; Rare:143 | ||||
| chr22:37560313-37560516 | Common:1; Rare:67 | ||||
| chr22:37608679-37608883 | Common:1; Rare:61 | ||||
| chr22:37675400-37675710 | Common:4; Rare:89 | ||||
| chr22:37696804-37697069 | Common:3; Rare:74 | ||||
| chr22:37849297-37849480 | Rare:109 | ||||
| chr22:37953599-37953755 | Rare:68 | ||||
| chr22:38506264-38506630 | Common:1; Rare:119 | ||||
| chr22:38570154-38570500 | Common:5; Rare:65 |