| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:227563868-227563997 | Common:1; Rare:42 | ||||
| chr1:227728020-227728065 | Rare:9 | ||||
| chr1:227728510-227728581 | Common:2; Rare:4 | ||||
| chr1:227735178-227735513 | Common:5; Rare:186 | ||||
| chr1:227947882-227948047 | Common:2; Rare:49 | ||||
| chr1:228082417-228082816 | Common:4; Rare:145 | ||||
| chr1:228083131-228083153 | Rare:7 | ||||
| chr1:228102891-228102949 | Rare:13 | ||||
| chr1:228103203-228103715 | Common:1; Rare:162 | ||||
| chr1:228109193-228109532 | Rare:108 | ||||
| chr1:228139785-228140382 | Common:4; Rare:181 | ||||
| chr1:228140455-228140638 | Common:1; Rare:38 | ||||
| chr1:228141717-228141804 | Rare:27 | ||||
| chr1:228165298-228165897 | Rare:183; Clinvar (benign):2 | ||||
| chr1:228165918-228166229 | Common:2; Rare:155; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):5 |