Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:53970979-53971101 | Common:3; Rare:49 | ||||
chr2:55232262-55232741 | Common:3; Rare:136 | ||||
chr2:61017440-61017750 | Common:1; Rare:93; Clinvar:2 | ||||
chr2:61144971-61145124 | Common:2; Rare:47 | ||||
chr2:61888385-61888703 | Common:1; Rare:144 | ||||
chr2:63588731-63589019 | Rare:89 | ||||
chr2:63841673-63841989 | Common:1; Rare:104 | ||||
chr2:65227591-65227870 | Rare:78 | ||||
chr2:68157478-68157955 | Common:2; Rare:247 | ||||
chr2:68467274-68467609 | Common:1; Rare:86 | ||||
chr2:70087340-70087918 | Common:2; Rare:202 | ||||
chr2:70087928-70088019 | Rare:25 | ||||
chr2:70293621-70293837 | Common:2; Rare:74 | ||||
chr2:71130220-71130327 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
chr2:74147821-74148127 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):2 |