| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:959217-959357 | Common:1; Rare:92 | ||||
| chr1:999986-1000519 | Common:9; Rare:179 | ||||
| chr1:1000702-1001012 | Common:3; Rare:80 | ||||
| chr1:1013289-1013731 | Common:6; Rare:121 | ||||
| chr1:1020047-1020337 | Common:4; Rare:91; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:1047609-1047895 | Common:3; Rare:126; Clinvar:11; Clinvar (benign):3 | ||||
| chr1:1048305-1048430 | Common:1; Rare:39; Clinvar:1 | ||||
| chr1:1049703-1050587 | Common:17; Rare:401; Clinvar:14; Clinvar (benign):22; Clinvar (pathogenic):1 | ||||
| chr1:1074302-1074483 | Common:3; Rare:42 | ||||
| chr1:1116063-1116427 | Common:1; Rare:113 | ||||
| chr1:1231891-1232326 | Rare:159; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr1:1273768-1274037 | Common:1; Rare:108 | ||||
| chr1:1307786-1308026 | Rare:53 | ||||
| chr1:1308333-1308658 | Common:8; Rare:140 | ||||
| chr1:1324594-1324932 | Common:3; Rare:160 |