Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:89955666-89955960 | Common:10; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
chr14:90331906-90332181 | Common:1; Rare:80 | ||||
chr14:91510285-91510624 | Common:1; Rare:103 | ||||
chr14:92040019-92040168 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
chr14:92121655-92121990 | Common:5; Rare:110 | ||||
chr14:92793995-92794408 | Rare:135 | ||||
chr14:93184851-93185013 | Rare:54 | ||||
chr14:93206991-93207290 | Common:2; Rare:147 | ||||
chr14:94081150-94081376 | Common:3; Rare:73 | ||||
chr14:96204726-96204926 | Common:4; Rare:81 | ||||
chr14:96363333-96363552 | Common:1; Rare:71 | ||||
chr14:96502301-96502446 | Rare:56 | ||||
chr14:99480769-99481018 | Common:2; Rare:96 | ||||
chr14:100375348-100375755 | Common:4; Rare:66 | ||||
chr14:100376259-100376495 | Common:3; Rare:77 |