| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:239386413-239386483 | Common:1; Rare:10 | ||||
| chr1:239386487-239386672 | Rare:27 | ||||
| chr1:240612007-240612163 | Rare:42 | ||||
| chr1:240612526-240612620 | Common:3; Rare:22 | ||||
| chr1:241519660-241519988 | Common:2; Rare:103; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr1:241848094-241848266 | Common:2; Rare:32 | ||||
| chr1:243254629-243254952 | Common:2; Rare:97 | ||||
| chr1:243255040-243255433 | Common:1; Rare:96 | ||||
| chr1:243255772-243256113 | Rare:96; Clinvar:4 | ||||
| chr1:243487674-243487852 | Common:3; Rare:48 | ||||
| chr1:244451807-244452214 | Common:1; Rare:137 | ||||
| chr1:244835008-244835333 | Rare:120 | ||||
| chr1:244835562-244835752 | Common:2; Rare:85; Clinvar (benign):5 | ||||
| chr1:244862996-244863315 | Common:4; Rare:130 | ||||
| chr1:244864009-244864254 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):5 |