| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74147810-74148052 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74178784-74179026 | Common:2; Rare:67 | ||||
| chr2:74198520-74198637 | Rare:56 | ||||
| chr2:74343364-74343667 | Common:1; Rare:53 | ||||
| chr2:74373198-74373424 | Common:1; Rare:45 | ||||
| chr2:74374321-74374439 | Rare:33; Clinvar:2 | ||||
| chr2:74391744-74392147 | Common:2; Rare:194 | ||||
| chr2:74421505-74421768 | Rare:82 | ||||
| chr2:74454871-74455341 | Rare:143 | ||||
| chr2:74458100-74458509 | Common:1; Rare:125 | ||||
| chr2:74459612-74459954 | Rare:108 | ||||
| chr2:74465206-74465455 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:74482916-74483142 | Common:1; Rare:88 | ||||
| chr2:74507327-74507463 | Rare:41 | ||||
| chr2:74507633-74507813 | Rare:43 |