| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151347182-151347492 | Rare:74 | ||||
| chr1:151399480-151399721 | Common:4; Rare:81; Clinvar (pathogenic):2 | ||||
| chr1:151511106-151511500 | Common:4; Rare:93 | ||||
| chr1:151540502-151540531 | Rare:6 | ||||
| chr1:151763135-151763608 | Common:3; Rare:194 | ||||
| chr1:151790426-151790871 | Common:3; Rare:108 | ||||
| chr1:151909397-151909615 | Common:2; Rare:87 | ||||
| chr1:151993752-151993994 | Common:4; Rare:88 | ||||
| chr1:152360003-152360136 | Rare:14 | ||||
| chr1:153535933-153536136 | Common:1; Rare:47 | ||||
| chr1:153536180-153536318 | Common:1; Rare:22 | ||||
| chr1:153540764-153540890 | Common:1; Rare:25 | ||||
| chr1:153544978-153545275 | Common:1; Rare:46 | ||||
| chr1:153545756-153545872 | Rare:20 | ||||
| chr1:153608916-153609041 | Common:1; Rare:19 |