Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:35290193-35290341 | Common:2; Rare:53 | ||||
chr18:36129301-36129471 | Common:1; Rare:51 | ||||
chr18:36129829-36129928 | Rare:41 | ||||
chr18:36828762-36829132 | Common:3; Rare:136 | ||||
chr18:46104137-46104396 | Common:3; Rare:74; Clinvar (benign):1 | ||||
chr18:47150452-47150546 | Common:2; Rare:34 | ||||
chr18:49561896-49562071 | Rare:43 | ||||
chr18:49813856-49814050 | Common:1; Rare:88 | ||||
chr18:49849806-49850088 | Common:2; Rare:68 | ||||
chr18:63422440-63422686 | Common:2; Rare:65 | ||||
chr18:63476825-63476980 | Rare:37 | ||||
chr18:68715057-68715173 | Rare:54 | ||||
chr18:70205664-70205809 | Common:3; Rare:57; Clinvar (benign):2 | ||||
chr18:74148358-74148546 | Common:1; Rare:58 | ||||
chr18:74291879-74292210 | Common:2; Rare:94 |