Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:73213008-73213362 | Common:1; Rare:69 | ||||
chr2:73984713-73984977 | Common:3; Rare:150 | ||||
chr2:73985179-73985501 | Common:6; Rare:156 | ||||
chr2:74120100-74120410 | Common:3; Rare:192 | ||||
chr2:74120430-74120800 | Common:14; Rare:188 | ||||
chr2:74377454-74378428 | Common:8; Rare:345; Clinvar:6; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
chr2:74489000-74489413 | Common:2; Rare:98 | ||||
chr2:74498139-74498539 | Rare:258 | ||||
chr2:74498549-74498700 | Common:2; Rare:37 | ||||
chr2:74501450-74501718 | Rare:68 | ||||
chr2:74940372-74940697 | Common:2; Rare:71 | ||||
chr2:75516300-75516740 | Common:2; Rare:137 | ||||
chr2:75522579-75523101 | Common:6; Rare:123 | ||||
chr2:75523480-75524068 | Common:6; Rare:178 | ||||
chr2:78541800-78542121 | Common:1; Rare:84 |