| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:18984021-18984199 | Rare:40 | ||||
| chrX:19343691-19344090 | Common:6; Rare:111; Clinvar (benign):1 | ||||
| chrX:19799745-19799825 | Rare:11 | ||||
| chrX:20141688-20142115 | Common:1; Rare:95 | ||||
| chrX:20218833-20219039 | Rare:38 | ||||
| chrX:21374126-21374477 | Common:2; Rare:79 | ||||
| chrX:21658262-21658529 | Common:1; Rare:58 | ||||
| chrX:21839490-21839669 | Rare:41 | ||||
| chrX:23667361-23667591 | Common:2; Rare:71 | ||||
| chrX:23743233-23743437 | Common:6; Rare:40 | ||||
| chrX:23782984-23783746 | Common:9; Rare:171 | ||||
| chrX:23785179-23785850 | Common:1; Rare:114 | ||||
| chrX:23907706-23907811 | Common:1; Rare:23 | ||||
| chrX:23907824-23908034 | Rare:38 | ||||
| chrX:24054883-24055031 | Rare:52 |