| ID: 130068728 | ATAC-STARR-seq lymphoblastoid silent region 21016 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134914921..134915090) | | |
| ID: 130068727 | ATAC-STARR-seq lymphoblastoid silent region 21015 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134810631..134810700) | | |
| ID: 130068726 | ATAC-STARR-seq lymphoblastoid active region 29977 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134807594..134807753) | | |
| ID: 130068725 | ATAC-STARR-seq lymphoblastoid silent region 21014 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134796901..134796980) | | |
| ID: 130068724 | ATAC-STARR-seq lymphoblastoid silent region 21013 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134796761..134796810) | | |
| ID: 129665007 | ReSE screen-validated silencer GRCh37_chrX:133966100-133966314 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134832070..134832284) | | |
| ID: 127898362 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:133942169-133943125 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134808139..134809095) | | |
| ID: 125467786 | Sharpr-MPRA regulatory region 6850 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134908419..134909147) | | |
| ID: 106479838 | RNA, U6 small nuclear 616, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134918310..134918416, complement) | | |
| ID: 106479578 | RNA, U4 small nuclear 44, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134760206..134760348, complement) | | |
| ID: 100270914 | ribosomal protein S7 pseudogene 12 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134650783..134651444) | RPS7_6_1816 | |
| ID: 159091 | PABIR family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134796364..134864771) | FAM122C | |
| ID: 159090 | PABIR family member 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134769566..134797205, complement) | FAM122B, SPACIA2 | |
| ID: 56180 | motile sperm domain containing 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134887632..134915257, complement) | DJ473B4 | 300674 |
| ID: 10761 | placenta enriched 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (134565838..134764322, complement) | CT92, OOSP2B, OOSP2L | 300296 |