| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137269389-137269640 | Rare:58 | ||||
| chr9:137322000-137322237 | Common:1; Rare:43 | ||||
| chr9:137498879-137499044 | Rare:39 | ||||
| chr9:137499107-137499393 | Common:1; Rare:72 | ||||
| chr9:137551984-137552135 | Rare:42 | ||||
| chrM:15884-16083 | |||||
| chrX:1387343-1387684 | Common:2; Rare:123 | ||||
| chrX:2609154-2609442 | Common:1; Rare:92 | ||||
| chrX:11221219-11221356 | Common:1; Rare:16 | ||||
| chrX:15675642-15675735 | Common:1; Rare:17 | ||||
| chrX:35625792-35625934 | Rare:46 | ||||
| chrX:47129748-47129947 | Common:1; Rare:18 | ||||
| chrX:47210845-47211225 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):5 | ||||
| chrX:47224696-47224850 | Rare:30 | ||||
| chrX:55489832-55490049 | Rare:25 |