| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:234523588-234524010 | Common:66; Rare:263 | ||||
| chr1:234600055-234600304 | Common:12; Rare:180 | ||||
| chr1:234610136-234610320 | Common:4; Rare:159 | ||||
| chr1:234610834-234611139 | Common:2; Rare:167 | ||||
| chr1:234612660-234612980 | Common:3; Rare:77 | ||||
| chr1:234724710-234725200 | Rare:135 | ||||
| chr1:234962090-234962800 | Common:2; Rare:150 | ||||
| chr1:234969610-234970594 | Common:8; Rare:266 | ||||
| chr1:234980680-234981200 | Rare:97 | ||||
| chr1:235068380-235068790 | Common:4; Rare:124 | ||||
| chr1:235070190-235070770 | Common:2; Rare:114 | ||||
| chr1:235073520-235073950 | Common:8; Rare:145 | ||||
| chr1:237470952-237471252 | Common:2; Rare:103 | ||||
| chr1:237496201-237496815 | Common:5; Rare:258; Clinvar:19; Clinvar (benign):6 | ||||
| chr1:238485973-238486079 | Common:1; Rare:26 |