| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27664125-27664287 | Common:1; Rare:58 | ||||
| chr2:27664362-27664548 | Rare:61 | ||||
| chr2:27890364-27890822 | Common:1; Rare:122 | ||||
| chr2:28392633-28392886 | Rare:90 | ||||
| chr2:28395520-28395735 | Common:1; Rare:45 | ||||
| chr2:28751674-28752176 | Common:2; Rare:209 | ||||
| chr2:28870256-28870454 | Rare:80 | ||||
| chr2:30146600-30147061 | Common:5; Rare:151 | ||||
| chr2:31138010-31138197 | Common:2; Rare:55 | ||||
| chr2:31233937-31234158 | Common:1; Rare:60 | ||||
| chr2:31414649-31414929 | Common:2; Rare:56; Clinvar (benign):1 | ||||
| chr2:32010961-32011107 | Rare:42 | ||||
| chr2:32039510-32039610 | Rare:24 | ||||
| chr2:32039732-32039860 | Rare:37 | ||||
| chr2:32063360-32063722 | Common:1; Rare:126; Clinvar:1 |