| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39575056-39575316 | Common:1; Rare:61 | ||||
| chr1:39576582-39576898 | Rare:102 | ||||
| chr1:39738689-39738966 | Common:2; Rare:73 | ||||
| chr1:39771281-39771358 | Common:3; Rare:20 | ||||
| chr1:39788815-39789212 | Common:5; Rare:119 | ||||
| chr1:39883440-39883637 | Common:1; Rare:74; Clinvar (pathogenic):1 | ||||
| chr1:39901989-39902120 | Rare:39 | ||||
| chr1:39954904-39955265 | Common:1; Rare:91 | ||||
| chr1:39955577-39955782 | Common:1; Rare:50 | ||||
| chr1:40039755-40040285 | Common:4; Rare:117 | ||||
| chr1:40040356-40040947 | Common:4; Rare:175 | ||||
| chr1:40097154-40097406 | Common:2; Rare:98; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr1:40161179-40161456 | Common:1; Rare:92 | ||||
| chr1:40161580-40161722 | Common:1; Rare:41 | ||||
| chr1:40257370-40258322 | Common:7; Rare:239; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):1 |