Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45396339-45396562 | Common:3; Rare:90 | ||||
chr19:46171270-46171309 | Rare:4 | ||||
chr19:46180815-46180930 | Rare:27 | ||||
chr19:46860910-46861115 | Common:1; Rare:70 | ||||
chr19:47107837-47108143 | Common:2; Rare:67 | ||||
chr19:49090311-49090470 | Rare:38 | ||||
chr19:50205242-50205479 | Common:1; Rare:61 | ||||
chr19:51354193-51354488 | Common:4; Rare:104; Clinvar:1; Clinvar (benign):6 | ||||
chr19:54126248-54126609 | Common:2; Rare:113; Clinvar:1 | ||||
chr19:58550262-58550421 | Rare:53 | ||||
chr2:10793154-10793485 | Common:5; Rare:81 | ||||
chr2:20209392-20209606 | Common:1; Rare:42 | ||||
chr2:20221850-20221894 | Rare:7 | ||||
chr2:20447729-20447823 | Rare:24 | ||||
chr2:20447826-20448216 | Rare:133 |