Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113841706-113841785 | Common:3; Rare:11 | ||||
chr14:21308755-21309055 | Common:2; Rare:70 | ||||
chr14:22383849-22384056 | Common:1; Rare:40 | ||||
chr14:22771017-22771347 | Common:2; Rare:116 | ||||
chr14:24436990-24437062 | Rare:24 | ||||
chr14:24695494-24695673 | Rare:28 | ||||
chr14:34873997-34874202 | Rare:42 | ||||
chr14:34971970-34972250 | Rare:56 | ||||
chr14:35402085-35402239 | Common:4; Rare:34 | ||||
chr14:49633953-49634100 | Common:1; Rare:67; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49634320-49634485 | Common:1; Rare:79; Clinvar:8; Clinvar (benign):2 | ||||
chr14:49862861-49863137 | Common:1; Rare:90 | ||||
chr14:49864031-49864078 | Rare:6 | ||||
chr14:49868131-49868370 | Common:1; Rare:50 | ||||
chr14:50003298-50003582 | Common:2; Rare:77 |