| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19901948-19902005 | Common:1; Rare:13 | ||||
| chr2:19990085-19990211 | Rare:32 | ||||
| chr2:20051571-20051824 | Common:1; Rare:67 | ||||
| chr2:20350835-20351045 | Common:1; Rare:85 | ||||
| chr2:20446863-20447074 | Common:3; Rare:79 | ||||
| chr2:20651057-20651262 | Rare:65 | ||||
| chr2:20823056-20823186 | Common:1; Rare:47 | ||||
| chr2:23940363-23940514 | Common:3; Rare:53 | ||||
| chr2:24049649-24049743 | Rare:20 | ||||
| chr2:24076213-24076579 | Rare:98 | ||||
| chr2:24123355-24123487 | Common:1; Rare:30 | ||||
| chr2:25878453-25878763 | Common:3; Rare:98 | ||||
| chr2:25982466-25982614 | Common:1; Rare:37 | ||||
| chr2:26033774-26034159 | Common:4; Rare:140 | ||||
| chr2:26244592-26244943 | Common:2; Rare:127; Clinvar:5; Clinvar (benign):7 |