Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10209904-10210175 | Common:1; Rare:62 | ||||
chr1:10459233-10459317 | Rare:13 | ||||
chr1:10508634-10508857 | Rare:38 | ||||
chr1:10555769-10555948 | Common:1; Rare:38 | ||||
chr1:10599218-10599826 | Common:3; Rare:115; Clinvar:6; Clinvar (benign):1 | ||||
chr1:10900837-10901153 | Rare:61 | ||||
chr1:10901344-10901518 | Common:2; Rare:28 | ||||
chr1:10937401-10937627 | Common:1; Rare:51 | ||||
chr1:11099298-11099325 | Rare:6 | ||||
chr1:11719380-11719429 | Rare:13 | ||||
chr1:11736849-11737057 | Common:5; Rare:50 | ||||
chr1:11739002-11739045 | Common:1; Rare:7 | ||||
chr1:11859610-11859866 | Rare:35 | ||||
chr1:11908147-11908323 | Common:25; Rare:193 | ||||
chr1:11908802-11909113 | Common:2; Rare:88 |