| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36252847-36253140 | Rare:63 | ||||
| chr22:36387810-36387846 | Rare:6 | ||||
| chr22:36387887-36388374 | Common:3; Rare:134; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36528940-36528992 | Rare:20 | ||||
| chr22:36529064-36529536 | Common:6; Rare:146 | ||||
| chr22:37019415-37019848 | Common:5; Rare:127 | ||||
| chr22:37745942-37746285 | Common:4; Rare:121 | ||||
| chr22:37805322-37805589 | Rare:97 | ||||
| chr22:37849299-37849482 | Rare:108 | ||||
| chr22:37953589-37953802 | Rare:81 | ||||
| chr22:38110619-38110962 | Common:2; Rare:83 | ||||
| chr22:38294169-38294481 | Rare:114 | ||||
| chr22:38570169-38570469 | Common:4; Rare:55 | ||||
| chr22:38656299-38656741 | Common:1; Rare:123 | ||||
| chr22:38681780-38682438 | Common:3; Rare:226 |