Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:71320287-71320479 | Rare:59 | ||||
chr14:73458526-73458857 | Common:5; Rare:86 | ||||
chr14:73644901-73645030 | Common:2; Rare:36; Clinvar:2 | ||||
chr14:73886785-73886869 | Common:1; Rare:25 | ||||
chr14:73950163-73950323 | Common:3; Rare:68; Clinvar (benign):1 | ||||
chr14:74019263-74019360 | Rare:43 | ||||
chr14:74493568-74493781 | Common:3; Rare:79; Clinvar (benign):4 | ||||
chr14:74713075-74713207 | Rare:66 | ||||
chr14:75002746-75002947 | Common:1; Rare:56; Clinvar:2 | ||||
chr14:75660800-75660969 | Rare:42 | ||||
chr14:77377082-77377129 | Rare:15 | ||||
chr14:77457554-77457844 | Common:1; Rare:90 | ||||
chr14:77708000-77708114 | Rare:54 | ||||
chr14:81220871-81221097 | Common:1; Rare:106 | ||||
chr14:81324145-81324249 | Common:1; Rare:15 |