Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40257903-40258255 | Common:4; Rare:91; Clinvar:6 | ||||
chr1:40508647-40508789 | Common:3; Rare:38 | ||||
chr1:40531514-40531561 | Rare:17 | ||||
chr1:42335169-42335403 | Common:5; Rare:111 | ||||
chr1:42456004-42456577 | Common:1; Rare:166 | ||||
chr1:42463034-42463344 | Common:4; Rare:98 | ||||
chr1:42767023-42767309 | Common:4; Rare:88 | ||||
chr1:42817004-42817134 | Common:1; Rare:32 | ||||
chr1:42846412-42846646 | Common:1; Rare:63 | ||||
chr1:42958846-42959042 | Common:2; Rare:51; Clinvar:4; Clinvar (benign):3 | ||||
chr1:43358674-43359006 | Common:7; Rare:103 | ||||
chr1:43367937-43368190 | Rare:61 | ||||
chr1:43389768-43389945 | Common:3; Rare:74 | ||||
chr1:44674451-44674744 | Common:2; Rare:66 | ||||
chr1:44739674-44739864 | Common:1; Rare:67 |