| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:106860032-106860155 | Rare:30 | ||||
| chr9:107637718-107638013 | Common:1; Rare:69 | ||||
| chr9:114398452-114398678 | Common:2; Rare:59 | ||||
| chr9:129320850-129321016 | Rare:25 | ||||
| chr9:129488537-129488873 | Common:1; Rare:89 | ||||
| chr9:129489091-129489140 | Common:1; Rare:4 | ||||
| chr9:133349553-133350319 | Common:1; Rare:277 | ||||
| chr9:136726207-136726311 | Common:2; Rare:40 | ||||
| chrM:15883-16000 | |||||
| chrM:16376-16401 | |||||
| chrX:2609154-2609433 | Common:1; Rare:90 | ||||
| chrX:15675619-15675729 | Rare:22 | ||||
| chrX:24025668-24025774 | Rare:25 | ||||
| chrX:33726112-33726397 | Rare:37 | ||||
| chrX:47210859-47211192 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):5 |