Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74713070-74713200 | Rare:69 | ||||
chr14:75002731-75003023 | Common:1; Rare:102; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr14:75127001-75127128 | Rare:42 | ||||
chr14:75278745-75278832 | Rare:20 | ||||
chr14:75660813-75661020 | Rare:49 | ||||
chr14:75661175-75661299 | Common:2; Rare:32 | ||||
chr14:77098001-77098348 | Rare:107 | ||||
chr14:77377053-77377431 | Common:2; Rare:116 | ||||
chr14:77457556-77457877 | Common:1; Rare:94 | ||||
chr14:77457966-77458121 | Rare:39 | ||||
chr14:77707991-77708117 | Rare:59 | ||||
chr14:81220871-81221163 | Common:1; Rare:134 | ||||
chr14:90397008-90397163 | Common:5; Rare:81 | ||||
chr14:91510262-91510624 | Common:1; Rare:114 | ||||
chr14:92040013-92040124 | Common:3; Rare:39; Clinvar:3; Clinvar (benign):2 |