| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131361639-131361904 | Common:3; Rare:79 | ||||
| chr3:139538925-139539082 | Common:1; Rare:45 | ||||
| chr3:150408860-150409012 | Rare:45 | ||||
| chr3:152153129-152153379 | Rare:46 | ||||
| chr3:153155301-153155599 | Common:4; Rare:60 | ||||
| chr3:157174938-157175223 | Common:3; Rare:125 | ||||
| chr3:169764853-169764861 | Rare:4; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:177026431-177026580 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:194583894-194584034 | Common:7; Rare:49 | ||||
| chr3:195657926-195658136 | Common:11; Rare:37 | ||||
| chr3:196503078-196503148 | Rare:30 | ||||
| chr3:197627833-197628032 | Common:6; Rare:75 | ||||
| chr3:197850988-197851096 | Rare:18 | ||||
| chr4:212505-212633 | Common:1; Rare:30 | ||||
| chr4:760770-761012 | Common:1; Rare:78 |