| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10689892-10689997 | Common:2; Rare:41 | ||||
| chr2:10812688-10812967 | Common:3; Rare:110 | ||||
| chr2:11465848-11466220 | Common:5; Rare:117 | ||||
| chr2:11746401-11746648 | Common:1; Rare:68; Clinvar:2 | ||||
| chr2:12716620-12717060 | Common:3; Rare:135 | ||||
| chr2:12717865-12718020 | Common:1; Rare:37 | ||||
| chr2:12718177-12718554 | Common:2; Rare:117 | ||||
| chr2:17753123-17753401 | Common:3; Rare:74 | ||||
| chr2:17753721-17754174 | Common:4; Rare:143; Clinvar (benign):1 | ||||
| chr2:18560673-18560800 | Rare:34 | ||||
| chr2:19901628-19902051 | Common:2; Rare:175 | ||||
| chr2:19990062-19990188 | Rare:30 | ||||
| chr2:20051545-20051807 | Common:1; Rare:69 | ||||
| chr2:20350825-20351071 | Common:1; Rare:105 | ||||
| chr2:20446792-20447091 | Common:3; Rare:120 |