| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:211435250-211435650 | Common:7; Rare:131 | ||||
| chr2:211766738-211767146 | Common:4; Rare:138 | ||||
| chr2:211835700-211836252 | Common:3; Rare:197 | ||||
| chr2:211881546-211881733 | Common:1; Rare:34 | ||||
| chr2:211900051-211900185 | Common:2; Rare:30 | ||||
| chr2:211927760-211928220 | Common:2; Rare:82 | ||||
| chr2:211954762-211955076 | Rare:68 | ||||
| chr2:211955609-211955824 | Common:2; Rare:45 | ||||
| chr2:211957968-211958325 | Common:1; Rare:74 | ||||
| chr2:211976807-211977092 | Rare:56 | ||||
| chr2:212145789-212146084 | Rare:61 | ||||
| chr2:212224427-212224844 | Common:15; Rare:143 | ||||
| chr2:212315513-212315909 | Common:7; Rare:121 | ||||
| chr2:212330238-212330872 | Common:5; Rare:131 | ||||
| chr2:212502451-212503588 | Common:10; Rare:246 |