Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:55319056-55319237 | Common:3; Rare:44 | ||||
chr15:55408244-55408734 | Common:4; Rare:109 | ||||
chr15:55993563-55993928 | Common:1; Rare:112 | ||||
chr15:56918393-56918715 | Common:2; Rare:109 | ||||
chr15:58933557-58933775 | Common:2; Rare:96 | ||||
chr15:59372794-59373047 | Common:2; Rare:83 | ||||
chr15:60479072-60479206 | Common:2; Rare:53 | ||||
chr15:63042445-63042940 | Common:6; Rare:153; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr15:63048268-63048610 | Common:5; Rare:131; Clinvar:3; Clinvar (benign):2 | ||||
chr15:63504293-63504734 | Common:3; Rare:142 | ||||
chr15:63833904-63834053 | Common:1; Rare:59 | ||||
chr15:64093770-64094127 | Common:1; Rare:101 | ||||
chr15:64387631-64387858 | Common:2; Rare:74 | ||||
chr15:64703192-64703367 | Common:1; Rare:68 | ||||
chr15:65286868-65286947 | Rare:22 |