Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:96802619-96803409 | Common:3; Rare:157 | ||||
chr1:96803470-96803619 | Rare:27 | ||||
chr1:97101191-97101462 | Common:1; Rare:37 | ||||
chr1:97192968-97193180 | Rare:58; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr1:97208390-97208588 | Common:1; Rare:36 | ||||
chr1:97529747-97529788 | Common:3; Rare:20 | ||||
chr1:97653031-97653297 | Common:2; Rare:52 | ||||
chr1:97656839-97656985 | Rare:26 | ||||
chr1:97797033-97797235 | Common:2; Rare:35 | ||||
chr1:97901120-97901218 | Rare:10 | ||||
chr1:97983546-97983604 | Common:1; Rare:13 | ||||
chr1:97983986-97984098 | Rare:20 | ||||
chr1:97987918-97988063 | Rare:20 | ||||
chr1:98039019-98039054 | Rare:6 | ||||
chr1:98044243-98044283 | Rare:9 |