Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:89955846-89955948 | Common:4; Rare:34; Clinvar:3; Clinvar (benign):1 | ||||
chr14:90331913-90332181 | Common:1; Rare:75 | ||||
chr14:90396866-90397232 | Common:5; Rare:174; Clinvar (benign):2 | ||||
chr14:91113982-91114118 | Rare:39 | ||||
chr14:91510268-91510637 | Common:1; Rare:119 | ||||
chr14:91836400-91836681 | Common:13; Rare:48 | ||||
chr14:92040013-92040148 | Common:3; Rare:43; Clinvar:3; Clinvar (benign):2 | ||||
chr14:92121655-92121999 | Common:5; Rare:116 | ||||
chr14:92748594-92748827 | Rare:63 | ||||
chr14:92793998-92794408 | Rare:133 | ||||
chr14:92923047-92923153 | Common:3; Rare:25 | ||||
chr14:93184856-93185008 | Rare:47 | ||||
chr14:93206972-93207281 | Common:2; Rare:150 | ||||
chr14:93430616-93431000 | Rare:69 | ||||
chr14:94081135-94081387 | Common:4; Rare:78 |