Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178480687-178480799 | Rare:31 | ||||
chr2:180980827-180980968 | Rare:32 | ||||
chr2:181458103-181458152 | Rare:15 | ||||
chr2:181458159-181458194 | Rare:13 | ||||
chr2:181891647-181892030 | Common:4; Rare:156 | ||||
chr2:181892183-181892198 | Rare:2 | ||||
chr2:182716195-182716480 | Common:1; Rare:94 | ||||
chr2:184598150-184598478 | Common:2; Rare:84 | ||||
chr2:186485993-186486377 | Common:3; Rare:111 | ||||
chr2:186589887-186590009 | Rare:34 | ||||
chr2:187448240-187448348 | Rare:17 | ||||
chr2:187554284-187554569 | Common:1; Rare:54 | ||||
chr2:189580772-189580932 | Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
chr2:189783946-189784148 | Common:5; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
chr2:189784331-189784537 | Common:2; Rare:75; Clinvar:7; Clinvar (benign):1 |