Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140564308-140564549 | Common:1; Rare:57 | ||||
chr5:140564556-140564846 | Rare:76 | ||||
chr5:140647311-140647504 | Rare:89; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr5:140647538-140647896 | Common:5; Rare:151; Clinvar:4; Clinvar (benign):5 | ||||
chr5:140664790-140664926 | Common:2; Rare:39 | ||||
chr5:140691282-140691644 | Common:2; Rare:129; Clinvar:10; Clinvar (benign):2 | ||||
chr5:141320725-141320933 | Common:3; Rare:74 | ||||
chr5:141636805-141637011 | Common:2; Rare:91 | ||||
chr5:142324967-142325264 | Rare:100 | ||||
chr5:144170513-144170856 | Common:2; Rare:101 | ||||
chr5:148383872-148384033 | Rare:52 | ||||
chr5:149345345-149345537 | Common:1; Rare:65 | ||||
chr5:149550078-149550416 | Rare:56 | ||||
chr5:149550842-149551118 | Rare:68 | ||||
chr5:149551360-149551572 | Rare:45 |