Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244652496-244653432 | Common:38; Rare:1377 | ||||
chr1:244653410-244654528 | Common:16; Rare:630 | ||||
chr1:244834399-244835500 | Common:8; Rare:1148 | ||||
chr1:244835466-244835900 | Common:20; Rare:684; Clinvar:2; Clinvar (benign):32 | ||||
chr1:244836062-244836462 | Common:1; Rare:91 | ||||
chr1:244839411-244840413 | Common:8; Rare:320 | ||||
chr1:244860457-244861309 | Rare:259 | ||||
chr1:244862283-244862762 | Common:14; Rare:248; Clinvar:2; Clinvar (benign):2 | ||||
chr1:244862873-244863375 | Common:28; Rare:931 | ||||
chr1:244863299-244864055 | Common:8; Rare:481; Clinvar:17; Clinvar (benign):20; Clinvar (pathogenic):1 | ||||
chr1:244864110-244864860 | Common:7; Rare:1211; Clinvar:2; Clinvar (benign):4 | ||||
chr1:244969547-244969705 | Rare:41 | ||||
chr1:244969618-244969739 | Rare:31 | ||||
chr1:244969860-244970460 | Common:27; Rare:922 | ||||
chr1:244970470-244971270 | Common:38; Rare:844 |