Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169485713-169486139 | Common:1; Rare:125; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794868-169795094 | Common:3; Rare:58 | ||||
chr1:170074549-170074771 | Common:2; Rare:54 | ||||
chr1:170532074-170532388 | Common:4; Rare:131; Clinvar:2 | ||||
chr1:170663029-170663174 | Rare:36 | ||||
chr1:171207470-171207762 | Common:2; Rare:60 | ||||
chr1:171741918-171742103 | Common:1; Rare:61 | ||||
chr1:171781431-171781718 | Common:3; Rare:65 | ||||
chr1:171841401-171841581 | Common:2; Rare:56 | ||||
chr1:172444007-172444143 | Rare:45 | ||||
chr1:173477164-173477425 | Common:3; Rare:98 | ||||
chr1:173714866-173715069 | Common:1; Rare:47 | ||||
chr1:173824348-173824702 | Rare:68; Clinvar:1 | ||||
chr1:173867970-173868218 | Common:1; Rare:89 | ||||
chr1:173868314-173868380 | Rare:20 |