| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157089152-157089282 | Rare:47 | ||||
| chr3:157089533-157089839 | Common:1; Rare:46 | ||||
| chr3:157089856-157090126 | Common:1; Rare:35 | ||||
| chr3:157174851-157175253 | Common:3; Rare:174 | ||||
| chr3:159732283-159732396 | Common:1; Rare:19 | ||||
| chr3:159763049-159763141 | Rare:19 | ||||
| chr3:167864567-167864869 | Rare:57 | ||||
| chr3:168026825-168027046 | Rare:45 | ||||
| chr3:168051490-168051814 | Common:3; Rare:61 | ||||
| chr3:168249535-168249698 | Common:1; Rare:42 | ||||
| chr3:168249946-168250224 | Rare:70 | ||||
| chr3:169765047-169765215 | Rare:74; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:172319679-172319951 | Common:1; Rare:52 | ||||
| chr3:180975502-180975648 | Rare:26 | ||||
| chr3:183447404-183447715 | Common:3; Rare:78 |