Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:938680-938830 | Common:2; Rare:39 | ||||
chr1:1013389-1013549 | Common:4; Rare:54 | ||||
chr1:1324593-1324868 | Common:3; Rare:146 | ||||
chr1:1399266-1399589 | Common:1; Rare:151 | ||||
chr1:1658913-1659257 | Common:6; Rare:143 | ||||
chr1:1724280-1724465 | Common:3; Rare:66 | ||||
chr1:2194707-2194840 | Rare:46 | ||||
chr1:2391540-2391899 | Common:2; Rare:133 | ||||
chr1:3900219-3900383 | Common:10; Rare:81 | ||||
chr1:6199527-6199804 | Common:2; Rare:96 | ||||
chr1:6701769-6701981 | Rare:64 | ||||
chr1:7771177-7771363 | Common:3; Rare:84 | ||||
chr1:7961457-7961790 | Common:4; Rare:112; Clinvar:3; Clinvar (benign):3 | ||||
chr1:8878578-8878823 | Rare:125 | ||||
chr1:9942987-9943489 | Common:7; Rare:127 |