| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:167935735-167936291 | Common:3; Rare:162 | ||||
| chr1:167936543-167937003 | Common:1; Rare:166 | ||||
| chr1:167937495-167937724 | Rare:52 | ||||
| chr1:168136744-168137098 | Common:2; Rare:66 | ||||
| chr1:168178689-168179176 | Common:4; Rare:143 | ||||
| chr1:168225712-168226141 | Common:4; Rare:140 | ||||
| chr1:169106189-169106368 | Common:3; Rare:68 | ||||
| chr1:169367723-169368332 | Common:4; Rare:129 | ||||
| chr1:169485703-169486195 | Common:1; Rare:145; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:169486244-169486352 | Rare:22 | ||||
| chr1:169711590-169711734 | Rare:37 | ||||
| chr1:169794678-169794806 | Rare:21 | ||||
| chr1:169794847-169795126 | Common:3; Rare:75 | ||||
| chr1:170074440-170074757 | Common:2; Rare:101 | ||||
| chr1:170531943-170532376 | Common:5; Rare:152; Clinvar:2 |