Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16613499-16613703 | Common:3; Rare:1 | ||||
chr1:17054021-17054316 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):3 | ||||
chr1:17439747-17439871 | Rare:45 | ||||
chr1:19210251-19210410 | Rare:62 | ||||
chr1:19251512-19251848 | Common:6; Rare:109 | ||||
chr1:20508117-20508229 | Rare:31 | ||||
chr1:20661353-20661730 | Common:3; Rare:136; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787197-20787395 | Rare:100 | ||||
chr1:21345484-21345677 | Rare:72 | ||||
chr1:22052521-22052736 | Common:3; Rare:72 | ||||
chr1:22451742-22451868 | Common:1; Rare:51 | ||||
chr1:23344219-23344521 | Common:2; Rare:103 | ||||
chr1:23559407-23559657 | Common:1; Rare:107 | ||||
chr1:23691654-23691897 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23743269-23743503 | Rare:89 |