| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137188538-137188723 | Common:2; Rare:93 | ||||
| chr9:137618797-137619024 | Common:1; Rare:103 | ||||
| chrM:3204-3510 | |||||
| chrM:5576-5590 | |||||
| chrM:6945-7124 | |||||
| chrM:7968-8065 | |||||
| chrM:15138-15179 | |||||
| chrX:11111103-11111356 | Common:3; Rare:54 | ||||
| chrX:13688995-13689166 | Rare:41 | ||||
| chrX:13734529-13734849 | Common:3; Rare:98; Clinvar (benign):1 | ||||
| chrX:14873045-14873393 | Common:1; Rare:64 | ||||
| chrX:15790408-15790504 | Rare:28 | ||||
| chrX:17737183-17737488 | Common:3; Rare:28 | ||||
| chrX:19670887-19670990 | Rare:21 | ||||
| chrX:21940607-21940810 | Common:2; Rare:57 |