| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:204515516-204515916 | Common:1; Rare:78 | ||||
| chr1:204515964-204516103 | Rare:24 | ||||
| chr1:204516105-204516823 | Common:10; Rare:781 | ||||
| chr1:205121880-205122618 | Common:21; Rare:735 | ||||
| chr1:205172680-205173080 | Common:2; Rare:167 | ||||
| chr1:205211210-205211990 | Common:5; Rare:585; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr1:205227690-205228060 | Common:2; Rare:236 | ||||
| chr1:205229426-205230462 | Common:33; Rare:315 | ||||
| chr1:205255788-205256276 | Common:8; Rare:243 | ||||
| chr1:205321380-205321990 | Common:11; Rare:578 | ||||
| chr1:205449830-205450266 | Common:12; Rare:386 | ||||
| chr1:205450230-205450799 | Common:2; Rare:177 | ||||
| chr1:205591805-205592205 | Rare:250 | ||||
| chr1:205631237-205631724 | Common:27; Rare:557 | ||||
| chr1:205631630-205633051 | Common:30; Rare:1172 |