Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:99320869-99320962 | Rare:20 | ||||
chr13:99322325-99322454 | Rare:22 | ||||
chr13:110521973-110522232 | Common:1; Rare:38 | ||||
chr13:110897073-110897247 | Common:1; Rare:45 | ||||
chr13:113616602-113616857 | Common:2; Rare:54 | ||||
chr14:22771027-22771347 | Common:2; Rare:113 | ||||
chr14:22778650-22778934 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr14:24169590-24169766 | Rare:36 | ||||
chr14:35314361-35314531 | Common:2; Rare:32 | ||||
chr14:50003396-50003586 | Rare:54 | ||||
chr14:50040554-50040681 | Rare:14 | ||||
chr14:51884302-51884620 | Common:1; Rare:66 | ||||
chr14:52315388-52315715 | Rare:59 | ||||
chr14:54783303-54783357 | Rare:7 | ||||
chr14:55098439-55098598 | Common:1; Rare:32 |