| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11465120-11465418 | Common:3; Rare:68 | ||||
| chr2:11465804-11465990 | Rare:65 | ||||
| chr2:11466069-11466100 | Common:1; Rare:10 | ||||
| chr2:11466103-11466191 | Common:2; Rare:29 | ||||
| chr2:11746383-11746671 | Common:2; Rare:81; Clinvar:4 | ||||
| chr2:12716614-12717060 | Common:3; Rare:139 | ||||
| chr2:16665798-16666017 | Common:4; Rare:43 | ||||
| chr2:17753689-17754168 | Common:5; Rare:148; Clinvar (benign):1 | ||||
| chr2:18560673-18560808 | Rare:36 | ||||
| chr2:19358542-19358782 | Rare:54 | ||||
| chr2:19901652-19901830 | Common:1; Rare:92 | ||||
| chr2:19901953-19902131 | Common:3; Rare:55 | ||||
| chr2:19990046-19990211 | Rare:45 | ||||
| chr2:20051408-20051878 | Common:1; Rare:146 | ||||
| chr2:20350632-20351071 | Common:1; Rare:158 |