| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161201369-161201818 | Common:2; Rare:150 | ||||
| chr1:161223333-161223794 | Common:2; Rare:156; Clinvar:3 | ||||
| chr1:161224117-161224391 | Rare:105 | ||||
| chr1:161225697-161226143 | Common:20; Rare:130 | ||||
| chr1:161307392-161307616 | Rare:55; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:161314255-161314437 | Common:6; Rare:149; Clinvar:20; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr1:161750160-161750490 | Rare:84 | ||||
| chr1:161766129-161766376 | Common:6; Rare:141 | ||||
| chr1:162069566-162069816 | Common:2; Rare:129 | ||||
| chr1:162497752-162497888 | Common:3; Rare:91 | ||||
| chr1:162561312-162561729 | Common:8; Rare:269 | ||||
| chr1:162790499-162790836 | Common:9; Rare:189 | ||||
| chr1:163321693-163322104 | Common:2; Rare:207 | ||||
| chr1:165630753-165630896 | Common:1; Rare:85 | ||||
| chr1:165631095-165631286 | Common:4; Rare:62 |