| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161118022-161118136 | Rare:53 | ||||
| chr1:161159392-161159500 | Common:1; Rare:29 | ||||
| chr1:161314265-161314417 | Common:3; Rare:60; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:161631098-161631388 | Common:9; Rare:104 | ||||
| chr1:161766157-161766363 | Common:3; Rare:62 | ||||
| chr1:163202910-163203210 | Common:1; Rare:58 | ||||
| chr1:163321723-163322057 | Common:1; Rare:91 | ||||
| chr1:165768768-165768938 | Common:1; Rare:75 | ||||
| chr1:167935958-167936261 | Common:1; Rare:92 | ||||
| chr1:167936556-167936967 | Common:1; Rare:146 | ||||
| chr1:168225714-168226056 | Common:3; Rare:111 | ||||
| chr1:169367784-169368246 | Common:3; Rare:84 | ||||
| chr1:169427350-169427631 | Common:2; Rare:60 | ||||
| chr1:169794890-169795094 | Common:3; Rare:53 | ||||
| chr1:170531884-170532191 | Common:3; Rare:90; Clinvar:1 |