| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:44752515-44752613 | Common:2; Rare:40 | ||||
| chr22:45163798-45164003 | Common:2; Rare:76 | ||||
| chr22:45309690-45309978 | Common:1; Rare:115 | ||||
| chr22:46053783-46053878 | Rare:33 | ||||
| chr22:46267841-46268027 | Common:1; Rare:56 | ||||
| chr22:46296744-46296918 | Rare:57 | ||||
| chr22:46335601-46335753 | Common:2; Rare:64; Clinvar:6; Clinvar (benign):6 | ||||
| chr22:46762506-46762669 | Common:3; Rare:58 | ||||
| chr22:50244991-50245086 | Rare:38 | ||||
| chr22:50628150-50628306 | Common:7; Rare:75 | ||||
| chr22:50783592-50783842 | Common:2; Rare:84 | ||||
| chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr3:4303253-4303407 | Common:1; Rare:59 | ||||
| chr3:4493176-4493348 | Rare:61 | ||||
| chr3:4979183-4979530 | Common:2; Rare:76 |