| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25342463-25342715 | Common:1; Rare:59 | ||||
| chr2:25673483-25673757 | Common:1; Rare:106 | ||||
| chr2:25878304-25878357 | Rare:14 | ||||
| chr2:26033788-26034167 | Common:3; Rare:136 | ||||
| chr2:26034199-26034455 | Common:2; Rare:71 | ||||
| chr2:26034496-26034639 | Common:2; Rare:46 | ||||
| chr2:26194564-26194810 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244564-26245053 | Common:2; Rare:167; Clinvar:7; Clinvar (benign):9 | ||||
| chr2:26345802-26346187 | Common:1; Rare:114 | ||||
| chr2:26764188-26764346 | Common:1; Rare:62 | ||||
| chr2:27032831-27033011 | Rare:74 | ||||
| chr2:27071516-27071858 | Common:1; Rare:100 | ||||
| chr2:27086581-27086829 | Common:3; Rare:73; Clinvar (benign):3 | ||||
| chr2:27093944-27094154 | Common:1; Rare:41 | ||||
| chr2:27211744-27212065 | Common:3; Rare:111 |