| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:166875688-166875847 | Common:1; Rare:45 | ||||
| chr1:166876137-166876595 | Common:1; Rare:140 | ||||
| chr1:167219869-167220373 | Common:4; Rare:154 | ||||
| chr1:167220376-167220965 | Common:3; Rare:185 | ||||
| chr1:167221232-167221410 | Common:1; Rare:63 | ||||
| chr1:167439341-167439441 | Common:1; Rare:29; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr1:167553711-167553970 | Common:3; Rare:74 | ||||
| chr1:167721145-167721205 | Rare:8 | ||||
| chr1:167721722-167722039 | Common:4; Rare:87 | ||||
| chr1:167722419-167722474 | Common:1; Rare:17 | ||||
| chr1:167722571-167722641 | Common:1; Rare:21 | ||||
| chr1:167935372-167935636 | Common:1; Rare:43 | ||||
| chr1:167935849-167935939 | Rare:21 | ||||
| chr1:167935941-167936422 | Common:2; Rare:135 | ||||
| chr1:167936426-167936965 | Common:2; Rare:185 |