| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154535938-154536166 | Common:1; Rare:52; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chrX:156029022-156029364 | Common:5; Rare:21 | ||||
| chrY:3002793-3003005 | Rare:2 | ||||
| chrY:3072835-3073065 | |||||
| chrY:3622527-3622686 | |||||
| chrY:3786649-3786851 | |||||
| chrY:5925736-5925814 | |||||
| chrY:6266391-6266639 | |||||
| chrY:7803909-7804030 | Rare:1 | ||||
| chrY:8128059-8128375 | Rare:5 | ||||
| chrY:10035287-10035393 | Rare:1 | ||||
| chrY:12662164-12662506 | Rare:3 | ||||
| chrY:13000672-13000954 | Rare:2 | ||||
| chrY:13266750-13266813 | |||||
| chrY:13478511-13478570 | Rare:2 |