Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40374599-40374669 | Common:7; Rare:18 | ||||
chr1:40508662-40508807 | Common:4; Rare:40 | ||||
chr1:40531505-40531668 | Rare:38 | ||||
chr1:40691504-40691637 | Common:1; Rare:64 | ||||
chr1:40691639-40691860 | Common:1; Rare:91 | ||||
chr1:40692033-40692117 | Rare:35 | ||||
chr1:40979386-40979826 | Common:5; Rare:136 | ||||
chr1:42335106-42335395 | Common:6; Rare:141 | ||||
chr1:42335848-42336018 | Rare:33 | ||||
chr1:42456010-42456583 | Common:1; Rare:168 | ||||
chr1:42456940-42456973 | Rare:11 | ||||
chr1:42658273-42658452 | Common:2; Rare:51 | ||||
chr1:42682158-42682682 | Common:2; Rare:163 | ||||
chr1:42683161-42683466 | Common:3; Rare:141 | ||||
chr1:42766996-42767309 | Common:4; Rare:105; Clinvar (benign):1 |