Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1231886-1232284 | Rare:141; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:1273824-1274259 | Common:4; Rare:141 | ||||
chr1:1304650-1304970 | Common:2; Rare:94 | ||||
chr1:1305040-1305165 | Common:1; Rare:32 | ||||
chr1:1305665-1305789 | Rare:45 | ||||
chr1:1308363-1308668 | Common:8; Rare:134 | ||||
chr1:1324593-1324882 | Common:3; Rare:150 | ||||
chr1:1348773-1349173 | Common:1; Rare:198 | ||||
chr1:1349372-1349612 | Common:2; Rare:84 | ||||
chr1:1375139-1375632 | Common:7; Rare:142 | ||||
chr1:1399272-1399611 | Common:1; Rare:158 | ||||
chr1:1407152-1407447 | Common:1; Rare:126 | ||||
chr1:1434396-1434539 | Rare:43 | ||||
chr1:1435220-1435780 | Rare:155 | ||||
chr1:1471558-1471797 | Common:5; Rare:94 |