| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10812704-10812967 | Common:3; Rare:105 | ||||
| chr2:11746500-11746655 | Common:1; Rare:47; Clinvar:2 | ||||
| chr2:12716608-12717076 | Common:4; Rare:146 | ||||
| chr2:12717703-12717849 | Rare:29 | ||||
| chr2:12718189-12718242 | Common:1; Rare:7 | ||||
| chr2:15561301-15561427 | Rare:51 | ||||
| chr2:17540469-17540555 | Common:1; Rare:10 | ||||
| chr2:17540562-17540897 | Common:2; Rare:79 | ||||
| chr2:17753711-17754169 | Common:4; Rare:143; Clinvar (benign):1 | ||||
| chr2:18560673-18560805 | Rare:35 | ||||
| chr2:19901628-19901743 | Common:1; Rare:60 | ||||
| chr2:19901925-19902037 | Common:1; Rare:36 | ||||
| chr2:19990062-19990195 | Rare:34 | ||||
| chr2:20350656-20351050 | Common:1; Rare:140 | ||||
| chr2:20446854-20447074 | Common:3; Rare:88 |