Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:146182589-146182854 | Common:2; Rare:68 | ||||
chr5:149345339-149345524 | Common:1; Rare:57 | ||||
chr5:149551369-149551630 | Rare:60 | ||||
chr5:150449662-150449795 | Common:4; Rare:46 | ||||
chr5:150701021-150701160 | Common:2; Rare:50 | ||||
chr5:151080976-151081202 | Common:1; Rare:75 | ||||
chr5:154038887-154038989 | Rare:31 | ||||
chr5:159263201-159263294 | Common:1; Rare:26 | ||||
chr5:160419053-160419171 | Common:2; Rare:33 | ||||
chr5:163437335-163437607 | Rare:80 | ||||
chr5:176361739-176361885 | Rare:42 | ||||
chr5:176388558-176388780 | Common:1; Rare:78 | ||||
chr5:177022634-177022732 | Rare:32 | ||||
chr5:177351650-177351766 | Rare:26 | ||||
chr5:177516941-177517093 | Rare:49; Clinvar (pathogenic):1 |