Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155944740-155945060 | Common:2; Rare:118 | ||||
chr1:156118349-156118982 | Common:6; Rare:145 | ||||
chr1:156130301-156130730 | Common:5; Rare:179; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):8 | ||||
chr1:156456450-156456870 | Common:4; Rare:157 | ||||
chr1:156661320-156661635 | Common:2; Rare:100 | ||||
chr1:160030580-160031160 | Common:3; Rare:231; Clinvar:1; Clinvar (benign):2 | ||||
chr1:161217201-161217588 | Common:4; Rare:116 | ||||
chr1:161218598-161219025 | Common:6; Rare:292 | ||||
chr1:161222590-161222890 | Common:1; Rare:47 | ||||
chr1:161389880-161390250 | Common:13; Rare:152 | ||||
chr1:161399190-161399500 | Common:2; Rare:113 | ||||
chr1:161399520-161399950 | Common:13; Rare:346 | ||||
chr1:161726912-161727312 | Common:14; Rare:221 | ||||
chr1:165598130-165598390 | Common:16; Rare:96 | ||||
chr1:167221835-167222235 | Common:2; Rare:177 |