| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231211415-231211659 | Common:1; Rare:66 | ||||
| chr1:231241844-231241910 | Common:1; Rare:10 | ||||
| chr1:231340096-231340151 | Common:1; Rare:10 | ||||
| chr1:231340614-231340645 | Rare:5 | ||||
| chr1:231359249-231359322 | Common:1; Rare:19 | ||||
| chr1:231395483-231395746 | Common:4; Rare:42 | ||||
| chr1:231395818-231395984 | Common:1; Rare:25 | ||||
| chr1:231420879-231420957 | Rare:23 | ||||
| chr1:231421187-231421435 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr1:231421481-231421778 | Common:2; Rare:98; Clinvar:8; Clinvar (benign):5 | ||||
| chr1:231421987-231422786 | Common:7; Rare:289; Clinvar:11; Clinvar (benign):8 | ||||
| chr1:231627474-231627523 | Rare:6 | ||||
| chr1:231800136-231800367 | Common:1; Rare:68; Clinvar:1 | ||||
| chr1:231827655-231827697 | Rare:8 | ||||
| chr1:231828230-231828465 | Common:1; Rare:26 |