| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:94926862-94926910 | Rare:12 | ||||
| chr1:94926961-94927019 | Common:1; Rare:11 | ||||
| chr1:95072863-95073018 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr1:95233945-95234233 | Common:5; Rare:84 | ||||
| chr1:96721683-96721867 | Common:1; Rare:79 | ||||
| chr1:98661596-98661869 | Common:2; Rare:98 | ||||
| chr1:99766620-99766729 | Rare:22 | ||||
| chr1:99849863-99850123 | Common:2; Rare:81 | ||||
| chr1:99850336-99850402 | Rare:19; Clinvar:1 | ||||
| chr1:99969907-99970122 | Rare:55 | ||||
| chr1:100037996-100038185 | Common:1; Rare:76 | ||||
| chr1:100132911-100133214 | Common:2; Rare:110 | ||||
| chr1:100249807-100249982 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:100266107-100266378 | Common:3; Rare:96 | ||||
| chr1:100894647-100894914 | Common:2; Rare:65 |