| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:164558887-164559184 | Common:1; Rare:85 | ||||
| chr1:165631116-165631284 | Common:4; Rare:54 | ||||
| chr1:165698456-165698725 | Common:3; Rare:114 | ||||
| chr1:165768732-165769030 | Common:2; Rare:114 | ||||
| chr1:166839322-166839550 | Rare:64 | ||||
| chr1:167220534-167220925 | Common:2; Rare:121 | ||||
| chr1:167935958-167936261 | Common:1; Rare:92 | ||||
| chr1:167936566-167936974 | Common:1; Rare:146 | ||||
| chr1:168178724-168179109 | Common:4; Rare:119 | ||||
| chr1:168225712-168226072 | Common:4; Rare:114 | ||||
| chr1:169367764-169368250 | Common:3; Rare:93 | ||||
| chr1:169427336-169427526 | Common:2; Rare:40 | ||||
| chr1:169485685-169486234 | Common:2; Rare:159; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:169794868-169795053 | Common:3; Rare:39 | ||||
| chr1:170074557-170074847 | Common:2; Rare:76 |