Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:197791169-197791290 | Common:2; Rare:50 | ||||
chr3:197949861-197950250 | Common:4; Rare:116; Clinvar (benign):2 | ||||
chr3:197959969-197960245 | Common:1; Rare:96 | ||||
chr4:337632-337860 | Rare:67 | ||||
chr4:499124-499301 | Common:3; Rare:71 | ||||
chr4:673842-673975 | Rare:53 | ||||
chr4:674234-674608 | Common:3; Rare:175 | ||||
chr4:689152-689422 | Common:3; Rare:69 | ||||
chr4:932259-932487 | Common:2; Rare:88 | ||||
chr4:1113524-1113578 | Common:1; Rare:16 | ||||
chr4:1309400-1309621 | Common:3; Rare:57 | ||||
chr4:2468888-2469154 | Common:2; Rare:95 | ||||
chr4:2843678-2844014 | Common:3; Rare:123 | ||||
chr4:2934767-2934894 | Common:1; Rare:58 | ||||
chr4:2963315-2963587 | Common:2; Rare:102 |