Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:81221285-81221495 | Common:1; Rare:61 | ||||
chr14:81324158-81324259 | Common:1; Rare:13 | ||||
chr14:85530004-85530194 | Common:1; Rare:40 | ||||
chr14:87993052-87993294 | Common:4; Rare:112; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr14:88792864-88793063 | Rare:69 | ||||
chr14:88824309-88824806 | Common:2; Rare:148; Clinvar:3; Clinvar (benign):1 | ||||
chr14:89350277-89350317 | Rare:11 | ||||
chr14:89619126-89619260 | Rare:52 | ||||
chr14:90331921-90332181 | Common:1; Rare:69 | ||||
chr14:90396870-90397114 | Common:2; Rare:127 | ||||
chr14:91060565-91060880 | Common:2; Rare:96 | ||||
chr14:91510254-91510624 | Common:1; Rare:116 | ||||
chr14:91836404-91836693 | Common:12; Rare:53 | ||||
chr14:92039838-92040134 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
chr14:92121647-92121990 | Common:5; Rare:112 |