Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:179604620-179604827 | Common:1; Rare:70 | ||||
chr3:180602020-180602209 | Common:1; Rare:53 | ||||
chr3:183253039-183253293 | Common:3; Rare:75 | ||||
chr3:183884850-183884959 | Rare:46 | ||||
chr3:184249531-184249768 | Common:1; Rare:77 | ||||
chr3:184298944-184299283 | Common:3; Rare:106 | ||||
chr3:186567309-186567403 | Common:3; Rare:20 | ||||
chr3:188153771-188153881 | Common:1; Rare:19 | ||||
chr3:188154067-188154212 | Rare:38 | ||||
chr3:193593142-193593303 | Rare:47; Clinvar:1 | ||||
chr3:196503762-196504045 | Common:5; Rare:92 | ||||
chr3:196568518-196568673 | Common:3; Rare:40 | ||||
chr3:197949893-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
chr4:499149-499319 | Common:2; Rare:59 | ||||
chr4:674252-674542 | Rare:133 |