Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9003953-9004090 | Rare:56 | ||||
chr2:9422816-9422874 | Rare:7 | ||||
chr2:9423136-9423697 | Common:1; Rare:153 | ||||
chr2:9473386-9473662 | Common:1; Rare:50 | ||||
chr2:9473667-9473776 | Rare:26 | ||||
chr2:9474484-9474642 | Common:6; Rare:72 | ||||
chr2:9555621-9556029 | Common:2; Rare:136 | ||||
chr2:9630944-9631316 | Common:3; Rare:119 | ||||
chr2:9843392-9843553 | Common:5; Rare:45 | ||||
chr2:9843645-9843721 | Common:2; Rare:29 | ||||
chr2:10043318-10043678 | Common:4; Rare:145; Clinvar:2; Clinvar (benign):1 | ||||
chr2:10448416-10448731 | Common:1; Rare:108 | ||||
chr2:10689910-10690024 | Common:2; Rare:40 | ||||
chr2:10812680-10813004 | Common:3; Rare:120 | ||||
chr2:11344973-11345060 | Common:2; Rare:34 |