Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593641-63593701 | Rare:33; Clinvar (pathogenic):1 | ||||
chr1:64841247-64841538 | Rare:67; Clinvar:2 | ||||
chr1:65792270-65792539 | Rare:60 | ||||
chr1:66533338-66534294 | Common:4; Rare:195 | ||||
chr1:66694460-66694951 | Common:3; Rare:115 | ||||
chr1:66695130-66695482 | Common:3; Rare:86 | ||||
chr1:66924787-66925031 | Common:1; Rare:108 | ||||
chr1:66930036-66930399 | Rare:122 | ||||
chr1:67053941-67053963 | Rare:7 | ||||
chr1:67424885-67425211 | Rare:81 | ||||
chr1:67430130-67430478 | Rare:133 | ||||
chr1:67684964-67685316 | Common:2; Rare:103 | ||||
chr1:67685432-67685468 | Rare:15 | ||||
chr1:67833339-67833575 | Common:3; Rare:91 | ||||
chr1:68232200-68232256 | Rare:16 |