| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017419-61017770 | Common:1; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144901-61145165 | Common:3; Rare:90 | ||||
| chr2:61888503-61888757 | Common:2; Rare:104 | ||||
| chr2:63588744-63589022 | Rare:86 | ||||
| chr2:63840840-63841142 | Common:1; Rare:82 | ||||
| chr2:63841673-63841921 | Common:1; Rare:89 | ||||
| chr2:64019015-64019145 | Common:1; Rare:42 | ||||
| chr2:64524080-64524415 | Common:3; Rare:102 | ||||
| chr2:64653879-64654122 | Common:2; Rare:101 | ||||
| chr2:65056186-65056462 | Common:2; Rare:95 | ||||
| chr2:65227598-65227877 | Rare:80 | ||||
| chr2:66435079-66435173 | Rare:19 | ||||
| chr2:67397193-67397412 | Rare:68 | ||||
| chr2:68157472-68157983 | Common:3; Rare:264 | ||||
| chr2:68467267-68467629 | Common:1; Rare:97 |