| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37560331-37560547 | Common:1; Rare:73 | ||||
| chr22:37608895-37609053 | Common:1; Rare:44 | ||||
| chr22:37849316-37849476 | Rare:90 | ||||
| chr22:37953599-37953743 | Rare:61 | ||||
| chr22:37984530-37984622 | Rare:29 | ||||
| chr22:38181744-38182049 | Common:3; Rare:76; Clinvar:1 | ||||
| chr22:38201682-38202093 | Common:2; Rare:113 | ||||
| chr22:38570154-38570477 | Common:4; Rare:61 | ||||
| chr22:38656387-38656703 | Common:1; Rare:72 | ||||
| chr22:38681821-38681993 | Common:1; Rare:70 | ||||
| chr22:39319596-39319785 | Common:3; Rare:88 | ||||
| chr22:39502193-39502379 | Rare:52 | ||||
| chr22:40044129-40044327 | Common:2; Rare:42 | ||||
| chr22:40346425-40346584 | Rare:74; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636647-40637033 | Common:2; Rare:107 |