| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201260429-201260611 | Rare:39 | ||||
| chr2:201272494-201272664 | Rare:29; Clinvar:1 | ||||
| chr2:201451416-201451910 | Common:3; Rare:124 | ||||
| chr2:201642633-201642775 | Rare:70 | ||||
| chr2:201643410-201643504 | Common:1; Rare:33; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:201780491-201780562 | Rare:27 | ||||
| chr2:201780876-201781243 | Common:3; Rare:112; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202265625-202265901 | Rare:98 | ||||
| chr2:202376420-202376609 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:202377038-202377393 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:202634945-202635019 | Common:5; Rare:30 | ||||
| chr2:202911606-202912024 | Common:1; Rare:87 | ||||
| chr2:202912128-202912304 | Common:2; Rare:58 | ||||
| chr2:202912474-202912580 | Common:2; Rare:36 | ||||
| chr2:203014672-203014952 | Common:1; Rare:85 |