| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9630944-9631316 | Common:3; Rare:119 | ||||
| chr2:9843254-9843553 | Common:6; Rare:89 | ||||
| chr2:10689901-10690032 | Common:2; Rare:48 | ||||
| chr2:10812683-10813020 | Common:3; Rare:126 | ||||
| chr2:11132771-11133112 | Common:5; Rare:74 | ||||
| chr2:11746347-11746661 | Common:2; Rare:85; Clinvar:3 | ||||
| chr2:12716602-12717062 | Common:4; Rare:144 | ||||
| chr2:12718173-12718270 | Common:1; Rare:20 | ||||
| chr2:14632405-14632807 | Common:1; Rare:134 | ||||
| chr2:15561294-15561427 | Rare:52 | ||||
| chr2:15940346-15940564 | Rare:53 | ||||
| chr2:17540500-17540934 | Common:3; Rare:95 | ||||
| chr2:17753682-17754174 | Common:5; Rare:153; Clinvar (benign):1 | ||||
| chr2:18560673-18560801 | Rare:34 | ||||
| chr2:19901609-19902051 | Common:2; Rare:181 |