| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:226985818-226985953 | Common:2; Rare:46 | ||||
| chr1:226986147-226986261 | Common:1; Rare:37 | ||||
| chr1:226986439-226986452 | Common:1; Rare:5; Clinvar (benign):1 | ||||
| chr1:226988238-226988438 | Common:2; Rare:62 | ||||
| chr1:227298559-227298710 | Common:1; Rare:20 | ||||
| chr1:227299295-227299419 | Common:1; Rare:17 | ||||
| chr1:227299758-227300009 | Common:3; Rare:44 | ||||
| chr1:227316162-227316291 | Common:1; Rare:26 | ||||
| chr1:227318998-227319079 | Rare:21 | ||||
| chr1:227319204-227319397 | Common:3; Rare:51 | ||||
| chr1:227333595-227333758 | Common:1; Rare:37 | ||||
| chr1:227344164-227344225 | Rare:11 | ||||
| chr1:227356651-227356873 | Common:3; Rare:40 | ||||
| chr1:227357553-227357649 | Rare:23 | ||||
| chr1:227542599-227542865 | Common:5; Rare:60 |