| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200306757-200306898 | Rare:43 | ||||
| chr2:200510040-200510236 | Common:1; Rare:61 | ||||
| chr2:200526016-200526230 | Common:3; Rare:63 | ||||
| chr2:200811403-200811572 | Common:1; Rare:58 | ||||
| chr2:200864229-200864277 | Rare:19 | ||||
| chr2:200864552-200864788 | Common:1; Rare:85 | ||||
| chr2:200889005-200889445 | Common:3; Rare:142 | ||||
| chr2:200963604-200963785 | Common:1; Rare:47 | ||||
| chr2:201071569-201072047 | Rare:108 | ||||
| chr2:201115880-201116202 | Common:2; Rare:59 | ||||
| chr2:201116267-201116436 | Rare:33 | ||||
| chr2:201451358-201451914 | Common:3; Rare:138 | ||||
| chr2:201642627-201642752 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr2:201643423-201643553 | Rare:42; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:201780876-201781241 | Common:3; Rare:112; Clinvar:3; Clinvar (benign):2 |