| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:119318390-119318870 | Common:19; Rare:278 | ||||
| chr1:119323640-119324160 | Rare:167 | ||||
| chr1:119327047-119327548 | Common:3; Rare:237 | ||||
| chr1:119327820-119328180 | Common:1; Rare:78 | ||||
| chr1:119347920-119348340 | Common:2; Rare:78 | ||||
| chr1:119648427-119648546 | Common:1; Rare:36 | ||||
| chr1:119712509-119712940 | Common:2; Rare:182 | ||||
| chr1:119736901-119737501 | Common:4; Rare:284; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr1:120340890-120341096 | Common:2; Rare:124 | ||||
| chr1:120341826-120341945 | Rare:31 | ||||
| chr1:120341993-120342424 | Rare:124 | ||||
| chr1:120415745-120415860 | Common:4; Rare:47 | ||||
| chr1:120415766-120415933 | Common:2; Rare:37 | ||||
| chr1:120558519-120558847 | Common:1; Rare:136 | ||||
| chr1:120844107-120844569 | Rare:86 |