| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161226728-161227048 | Rare:78 | ||||
| chr1:161307407-161307628 | Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:161314141-161314517 | Common:5; Rare:129; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr1:161314800-161314922 | Rare:30 | ||||
| chr1:161506652-161506831 | Common:1; Rare:37 | ||||
| chr1:161524353-161524546 | Common:3; Rare:65 | ||||
| chr1:161710665-161710808 | Common:2; Rare:54 | ||||
| chr1:161749614-161749937 | Rare:116 | ||||
| chr1:161749973-161750043 | Rare:29 | ||||
| chr1:161750181-161750384 | Rare:52 | ||||
| chr1:161766105-161766388 | Common:3; Rare:87 | ||||
| chr1:162023626-162023998 | Common:1; Rare:109 | ||||
| chr1:162024283-162024476 | Common:2; Rare:36 | ||||
| chr1:162069562-162069826 | Common:1; Rare:68 | ||||
| chr1:162497663-162497923 | Common:3; Rare:78 |