| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177392632-177392863 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:178451090-178451369 | Common:6; Rare:83; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:180007080-180007406 | Common:1; Rare:77 | ||||
| chr2:181457230-181457417 | Rare:65 | ||||
| chr2:181891908-181892217 | Common:1; Rare:105 | ||||
| chr2:186485987-186486354 | Common:3; Rare:105 | ||||
| chr2:186589925-186590057 | Rare:40 | ||||
| chr2:186590066-186590465 | Rare:134 | ||||
| chr2:188291410-188292060 | Common:7; Rare:176 | ||||
| chr2:188292676-188292855 | Common:1; Rare:43 | ||||
| chr2:188293001-188293071 | Rare:8 | ||||
| chr2:189783956-189784131 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784276-189784512 | Common:3; Rare:77; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190343875-190343938 | Rare:9 | ||||
| chr2:190534688-190534857 | Common:1; Rare:57 |