| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10689934-10690004 | Common:2; Rare:22 | ||||
| chr2:11344960-11345072 | Common:2; Rare:41 | ||||
| chr2:11466127-11466184 | Rare:15 | ||||
| chr2:11746422-11746648 | Common:1; Rare:64; Clinvar:2 | ||||
| chr2:12716756-12716975 | Common:1; Rare:59 | ||||
| chr2:17753112-17753408 | Common:4; Rare:77 | ||||
| chr2:17753627-17754159 | Common:4; Rare:169; Clinvar (benign):1 | ||||
| chr2:19901652-19901792 | Common:1; Rare:77 | ||||
| chr2:19901944-19902019 | Common:1; Rare:20 | ||||
| chr2:19990079-19990211 | Rare:34 | ||||
| chr2:20051541-20051824 | Common:1; Rare:80 | ||||
| chr2:20225128-20225257 | Common:1; Rare:29 | ||||
| chr2:20225369-20225619 | Common:1; Rare:62 | ||||
| chr2:20350807-20351071 | Common:1; Rare:113 | ||||
| chr2:20446887-20447117 | Common:3; Rare:90 |