Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:172555922-172556141 | Common:1; Rare:82 | ||||
chr2:173075543-173075891 | Common:3; Rare:95 | ||||
chr2:173965286-173965512 | Common:1; Rare:82 | ||||
chr2:174395629-174395812 | Common:1; Rare:60 | ||||
chr2:176002221-176002406 | Common:3; Rare:79 | ||||
chr2:177263412-177263603 | Rare:42 | ||||
chr2:177264646-177264826 | Common:2; Rare:59 | ||||
chr2:177392669-177393090 | Common:2; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
chr2:178451041-178451439 | Common:8; Rare:118; Clinvar:4; Clinvar (benign):4 | ||||
chr2:178478518-178478611 | Rare:33 | ||||
chr2:182716760-182717061 | Common:1; Rare:65 | ||||
chr2:183038020-183038058 | Rare:11 | ||||
chr2:186486118-186486445 | Common:3; Rare:108 | ||||
chr2:186505499-186505836 | Rare:83 | ||||
chr2:186589762-186590088 | Rare:93 |