| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39672066-39672138 | Common:1; Rare:24 | ||||
| chr1:39738744-39738898 | Common:2; Rare:32 | ||||
| chr1:40040457-40040788 | Common:3; Rare:98 | ||||
| chr1:40161252-40161394 | Rare:35 | ||||
| chr1:40257856-40258255 | Common:4; Rare:101; Clinvar:7 | ||||
| chr1:40508662-40508799 | Common:4; Rare:37 | ||||
| chr1:40531514-40531562 | Rare:17 | ||||
| chr1:40691602-40691836 | Common:1; Rare:111 | ||||
| chr1:42335169-42335282 | Common:1; Rare:49 | ||||
| chr1:42456033-42456349 | Common:1; Rare:80 | ||||
| chr1:42766514-42766722 | Rare:52; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:42767010-42767303 | Common:4; Rare:92; Clinvar (benign):1 | ||||
| chr1:42816985-42817164 | Common:1; Rare:54 | ||||
| chr1:42846398-42846655 | Common:1; Rare:73 | ||||
| chr1:42958830-42959084 | Common:4; Rare:71; Clinvar:6; Clinvar (benign):4 |