| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161238024-161238169 | Rare:31 | ||||
| chr2:161238810-161238843 | Rare:10 | ||||
| chr2:161243325-161243553 | Rare:39 | ||||
| chr2:161244481-161244562 | Rare:11 | ||||
| chr2:161244567-161244795 | Common:1; Rare:59 | ||||
| chr2:161244921-161245005 | Rare:9 | ||||
| chr2:161341349-161341357 | |||||
| chr2:162317861-162318050 | Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:162319680-162319713 | Rare:1 | ||||
| chr2:162732196-162732366 | Common:2; Rare:31 | ||||
| chr2:167862405-167862538 | Rare:25 | ||||
| chr2:168357925-168357949 | Rare:1 | ||||
| chr2:168457502-168457767 | Rare:51 | ||||
| chr2:168470960-168471173 | Common:6; Rare:38 | ||||
| chr2:168490012-168490219 | Common:3; Rare:32 |