| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:228140479-228140637 | Common:2; Rare:61 | ||||
| chr1:228144430-228144820 | Common:1; Rare:80 | ||||
| chr1:228146862-228148442 | Common:9; Rare:599 | ||||
| chr1:228165288-228165864 | Rare:302; Clinvar (benign):6 | ||||
| chr1:228165889-228166230 | Common:6; Rare:418; Clinvar:12; Clinvar (benign):21; Clinvar (pathogenic):15 | ||||
| chr1:228173999-228174630 | Common:31; Rare:362 | ||||
| chr1:228213082-228213448 | Common:3; Rare:104 | ||||
| chr1:228213480-228214020 | Common:14; Rare:326 | ||||
| chr1:228405698-228406317 | Common:10; Rare:208 | ||||
| chr1:228406663-228407254 | Common:16; Rare:315 | ||||
| chr1:228457440-228457705 | Common:1; Rare:180 | ||||
| chr1:228457810-228458194 | Common:5; Rare:471 | ||||
| chr1:228458493-228458914 | Common:17; Rare:269 | ||||
| chr1:228487007-228487488 | Common:14; Rare:394 | ||||
| chr1:228487700-228488410 | Common:10; Rare:281 |