| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:182061688-182061800 | Rare:21 | ||||
| chr1:182391295-182391538 | Common:1; Rare:59 | ||||
| chr1:182391750-182391972 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:182589003-182589323 | Common:1; Rare:61 | ||||
| chr1:182604340-182604600 | Rare:62 | ||||
| chr1:182839185-182839420 | Common:1; Rare:104 | ||||
| chr1:182839428-182839828 | Common:8; Rare:364 | ||||
| chr1:183023024-183023464 | Common:6; Rare:115 | ||||
| chr1:183186078-183186492 | Common:5; Rare:112; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:183471921-183472109 | Common:1; Rare:48 | ||||
| chr1:183472223-183472586 | Common:2; Rare:116 | ||||
| chr1:183635585-183635867 | Common:1; Rare:81 | ||||
| chr1:183804897-183804998 | Common:1; Rare:18 | ||||
| chr1:183805024-183805264 | Rare:66 | ||||
| chr1:184051107-184051300 | Common:1; Rare:27 |