Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15526556-15526905 | Common:2; Rare:111 | ||||
chr1:15758745-15758828 | Common:1; Rare:18 | ||||
chr1:16155946-16156191 | Rare:55; Clinvar:2 | ||||
chr1:16352420-16352606 | Common:3; Rare:99 | ||||
chr1:16440601-16440764 | Rare:51 | ||||
chr1:17053964-17054320 | Common:3; Rare:116; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17439669-17439875 | Rare:65 | ||||
chr1:19210251-19210410 | Rare:62 | ||||
chr1:19251498-19251854 | Common:6; Rare:119 | ||||
chr1:19311982-19312333 | Common:8; Rare:163 | ||||
chr1:20661340-20661754 | Common:3; Rare:151; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787196-20787395 | Rare:100 | ||||
chr1:21279462-21279731 | Rare:50 | ||||
chr1:21280024-21280135 | Common:1; Rare:14 | ||||
chr1:21290194-21290497 | Common:1; Rare:65 |