| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:234479103-234479231 | Common:5; Rare:51 | ||||
| chr1:234608010-234608500 | Common:3; Rare:275 | ||||
| chr1:235128669-235129060 | Common:1; Rare:274 | ||||
| chr1:235328109-235328617 | Common:8; Rare:283 | ||||
| chr1:235328659-235329059 | Common:2; Rare:202 | ||||
| chr1:235504369-235504791 | Common:10; Rare:259 | ||||
| chr1:235504830-235505270 | Common:2; Rare:109 | ||||
| chr1:235866858-235867144 | Common:6; Rare:167 | ||||
| chr1:236604408-236604680 | Common:9; Rare:156 | ||||
| chr1:236795067-236795457 | Common:11; Rare:268; Clinvar:6 | ||||
| chr1:236795710-236796170 | Common:3; Rare:169; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:241519661-241520019 | Common:4; Rare:219; Clinvar:22; Clinvar (benign):17; Clinvar (pathogenic):6 | ||||
| chr1:241639460-241639910 | Common:10; Rare:203 | ||||
| chr1:241640215-241640565 | Common:14; Rare:241 | ||||
| chr1:241640730-241641000 | Common:4; Rare:63 |