Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:176388547-176388811 | Common:4; Rare:105 | ||||
chr5:177022635-177022732 | Rare:32 | ||||
chr5:177133495-177133860 | Rare:134 | ||||
chr5:177303678-177304077 | Common:3; Rare:148 | ||||
chr5:177497536-177497798 | Common:1; Rare:98 | ||||
chr5:178153813-178154110 | Rare:90; Clinvar:5; Clinvar (benign):1 | ||||
chr5:179559488-179559793 | Common:1; Rare:96 | ||||
chr5:179698610-179699092 | Common:4; Rare:170 | ||||
chr5:179806321-179806448 | Rare:41 | ||||
chr5:180353321-180353490 | Common:4; Rare:69 | ||||
chr5:180810118-180810219 | Common:1; Rare:22 | ||||
chr5:180861214-180861435 | Common:2; Rare:92 | ||||
chr5:181223231-181223299 | Rare:20 | ||||
chr5:181261065-181261213 | Rare:44 | ||||
chr6:2245603-2245782 | Rare:54 |