Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92080174-92080614 | Common:3; Rare:114 | ||||
chr1:92080701-92080824 | Rare:44 | ||||
chr1:92298558-92299138 | Common:2; Rare:186; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92299483-92299521 | Rare:7 | ||||
chr1:92485874-92486014 | Rare:27 | ||||
chr1:92784653-92785620 | Common:9; Rare:266 | ||||
chr1:92831847-92832138 | Common:1; Rare:123; Clinvar:7; Clinvar (benign):7 | ||||
chr1:92832156-92832486 | Rare:105 | ||||
chr1:92832929-92832997 | Common:3; Rare:21 | ||||
chr1:92960981-92961144 | Common:1; Rare:39 | ||||
chr1:92961229-92962074 | Common:7; Rare:234 | ||||
chr1:93079008-93079409 | Common:4; Rare:155 | ||||
chr1:93079513-93079536 | Rare:1 | ||||
chr1:93179558-93180057 | Common:2; Rare:96 | ||||
chr1:93180096-93180557 | Rare:166 |