| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:10474854-10474984 | Rare:38; Clinvar:1 | ||||
| chr1:11099784-11099975 | Common:2; Rare:78 | ||||
| chr1:11262496-11262850 | Common:2; Rare:104 | ||||
| chr1:11654829-11654915 | Common:1; Rare:21 | ||||
| chr1:11735842-11736187 | Common:3; Rare:95 | ||||
| chr1:11805900-11806255 | Common:2; Rare:97; Clinvar:1 | ||||
| chr1:11934485-11934790 | Common:6; Rare:98; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:11980218-11980469 | Common:5; Rare:89; Clinvar:1; Clinvar (benign):4 | ||||
| chr1:12618124-12618444 | Common:2; Rare:67 | ||||
| chr1:13749188-13749445 | Common:2; Rare:88 | ||||
| chr1:15526589-15526913 | Common:2; Rare:102 | ||||
| chr1:15758740-15758817 | Common:1; Rare:18 | ||||
| chr1:16352420-16352594 | Common:3; Rare:92 | ||||
| chr1:16440564-16440774 | Common:1; Rare:62 | ||||
| chr1:17053976-17054368 | Common:3; Rare:118; Clinvar:12; Clinvar (benign):10 |