Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16366969-16367267 | Common:1; Rare:87 | ||||
chr1:16440544-16440770 | Common:1; Rare:64 | ||||
chr1:16613483-16613660 | Common:1 | ||||
chr1:16921814-16921931 | Rare:19 | ||||
chr1:17053991-17054331 | Common:3; Rare:100; Clinvar:6; Clinvar (benign):8 | ||||
chr1:17439652-17439877 | Rare:70 | ||||
chr1:19210247-19210428 | Rare:72 | ||||
chr1:19251498-19251863 | Common:6; Rare:122 | ||||
chr1:19312005-19312350 | Common:8; Rare:163 | ||||
chr1:19596866-19597087 | Common:2; Rare:104 | ||||
chr1:19771461-19771619 | Common:2; Rare:40 | ||||
chr1:20508079-20508237 | Common:2; Rare:56 | ||||
chr1:20661346-20661730 | Common:3; Rare:138; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787230-20787453 | Rare:108 | ||||
chr1:21176863-21177092 | Rare:59 |