Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89821500-89822120 | Common:5; Rare:277 | ||||
chr1:89843324-89843452 | Common:1; Rare:54 | ||||
chr1:89994973-89995218 | Common:4; Rare:167 | ||||
chr1:91021921-91022580 | Common:2; Rare:225 | ||||
chr1:91500740-91500991 | Common:4; Rare:134 | ||||
chr1:91501078-91501261 | Rare:46 | ||||
chr1:91885902-91886340 | Rare:295 | ||||
chr1:92080370-92080570 | Common:3; Rare:83 | ||||
chr1:92298893-92299118 | Common:2; Rare:166; Clinvar:3; Clinvar (benign):3 | ||||
chr1:92784948-92785271 | Common:6; Rare:172 | ||||
chr1:92831870-92832158 | Common:2; Rare:238; Clinvar:13; Clinvar (benign):12 | ||||
chr1:92832200-92832610 | Rare:177 | ||||
chr1:92961434-92961595 | Rare:101 | ||||
chr1:93079071-93079329 | Common:5; Rare:202 | ||||
chr1:93179463-93180010 | Common:3; Rare:127 |