| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:230977980-230978230 | Common:5; Rare:102 | ||||
| chr1:231020246-231020646 | Common:4; Rare:147 | ||||
| chr1:231053851-231054251 | Common:4; Rare:92 | ||||
| chr1:231211400-231211696 | Common:2; Rare:128 | ||||
| chr1:231215310-231215710 | Common:1; Rare:114 | ||||
| chr1:231421159-231421280 | Rare:34 | ||||
| chr1:231422184-231422640 | Common:13; Rare:372; Clinvar:15; Clinvar (benign):13 | ||||
| chr1:231493390-231494280 | Common:3; Rare:278 | ||||
| chr1:231507680-231508080 | Rare:73 | ||||
| chr1:231603708-231604178 | Common:1; Rare:83 | ||||
| chr1:232630118-232630288 | Rare:63 | ||||
| chr1:232805629-232805763 | Common:1; Rare:66 | ||||
| chr1:232901254-232901654 | Common:1; Rare:95 | ||||
| chr1:232904525-232904925 | Common:2; Rare:80 | ||||
| chr1:232923563-232923963 | Rare:76 |