| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:210232801-210232911 | Common:1; Rare:29 | ||||
| chr1:210328856-210329019 | Rare:57 | ||||
| chr1:210329261-210329334 | Rare:25 | ||||
| chr1:211258926-211259511 | Common:4; Rare:222 | ||||
| chr1:211326279-211326591 | Common:4; Rare:57 | ||||
| chr1:211326694-211326867 | Common:3; Rare:48 | ||||
| chr1:211346026-211346122 | Rare:19 | ||||
| chr1:211675409-211675799 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr1:212035488-212035801 | Common:2; Rare:88 | ||||
| chr1:212285063-212285373 | Common:2; Rare:90 | ||||
| chr1:212301764-212301876 | Rare:19 | ||||
| chr1:212414811-212414998 | Common:3; Rare:58 | ||||
| chr1:212624662-212624834 | Common:1; Rare:24 | ||||
| chr1:212791716-212791934 | Common:5; Rare:100 | ||||
| chr1:212847640-212847731 | Common:1; Rare:8 |