Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140807052-140807081 | Common:1; Rare:6 | ||||
chr5:141320739-141320998 | Common:3; Rare:84 | ||||
chr5:141618917-141619090 | Rare:61; Clinvar:5; Clinvar (benign):1 | ||||
chr5:141636818-141637012 | Common:1; Rare:79 | ||||
chr5:141923526-141923939 | Common:1; Rare:115 | ||||
chr5:142324973-142325293 | Rare:105 | ||||
chr5:143404442-143404617 | Common:2; Rare:36 | ||||
chr5:144170563-144170777 | Common:1; Rare:79 | ||||
chr5:145835269-145835472 | Common:1; Rare:50 | ||||
chr5:145937633-145937761 | Rare:32 | ||||
chr5:146182560-146182904 | Common:4; Rare:102 | ||||
chr5:147234866-147235098 | Common:2; Rare:63 | ||||
chr5:147831494-147831736 | Common:2; Rare:64; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr5:147831741-147831798 | Rare:8 | ||||
chr5:147831859-147831884 | Rare:2 |