| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:88947262-88947625 | Rare:65; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr10:88951820-88951899 | Rare:12 | ||||
| chr10:89412218-89412527 | Common:1; Rare:68 | ||||
| chr10:89829385-89829565 | Common:5; Rare:39 | ||||
| chr10:89887982-89888094 | Common:2; Rare:24 | ||||
| chr10:90076254-90076424 | Common:2; Rare:28 | ||||
| chr10:91032979-91033166 | Rare:35 | ||||
| chr10:91103030-91103168 | Common:2; Rare:19 | ||||
| chr10:91199099-91199285 | Common:2; Rare:29 | ||||
| chr10:92420567-92420796 | Common:1; Rare:42 | ||||
| chr10:92669735-92669782 | Common:2; Rare:9 | ||||
| chr10:93567971-93568121 | Rare:34 | ||||
| chr10:93961490-93961640 | Common:1; Rare:37 | ||||
| chr10:94107475-94107515 | Rare:5 | ||||
| chr10:94108765-94108921 | Rare:21 |