Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:24208995-24209200 | Rare:102 | ||||
chr10:24465983-24466132 | Rare:21 | ||||
chr10:24466217-24466590 | Rare:87 | ||||
chr10:24722905-24723036 | Rare:36 | ||||
chr10:24723150-24723490 | Common:3; Rare:129 | ||||
chr10:25016422-25016712 | Common:16; Rare:210 | ||||
chr10:25016855-25017255 | Common:8; Rare:176 | ||||
chr10:25062401-25063088 | Common:10; Rare:170 | ||||
chr10:26697180-26697496 | Common:6; Rare:118 | ||||
chr10:26697579-26697740 | Common:2; Rare:75; Clinvar (benign):2 | ||||
chr10:26697770-26698005 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
chr10:26733854-26734534 | Common:5; Rare:194 | ||||
chr10:27100403-27100587 | Common:6; Rare:110; Clinvar:8; Clinvar (benign):4 | ||||
chr10:27154218-27154517 | Rare:147 | ||||
chr10:27155139-27155429 | Common:11; Rare:187; Clinvar:10; Clinvar (benign):11 |