Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:231961643-231961748 | Rare:30; Clinvar:1 | ||||
chr2:232550550-232550716 | Rare:61 | ||||
chr2:232697130-232697376 | Common:2; Rare:78 | ||||
chr2:233060240-233060476 | Common:1; Rare:69 | ||||
chr2:233251510-233251687 | Common:2; Rare:59 | ||||
chr2:233854505-233854699 | Common:3; Rare:52 | ||||
chr2:237085748-237085946 | Common:2; Rare:68 | ||||
chr2:240025302-240025407 | Rare:44; Clinvar:4; Clinvar (benign):2 | ||||
chr2:240560756-240560868 | Rare:50 | ||||
chr2:241102277-241102360 | Common:2; Rare:32 | ||||
chr2:241149450-241149615 | Common:2; Rare:51 | ||||
chr2:241315178-241315401 | Common:4; Rare:71 | ||||
chr2:241315649-241315989 | Common:5; Rare:131 | ||||
chr2:241617493-241617613 | Common:1; Rare:29 | ||||
chr2:241637534-241637704 | Common:1; Rare:92 |