| ID: 130060166 | ATAC-STARR-seq lymphoblastoid silent region 8133 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7615092..7615141) | | |
| ID: 130060165 | ATAC-STARR-seq lymphoblastoid silent region 8132 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7614452..7614981) | | |
| ID: 130060164 | ATAC-STARR-seq lymphoblastoid active region 11635 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7580463..7580532) | | |
| ID: 130060163 | ATAC-STARR-seq lymphoblastoid active region 11634 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7580303..7580362) | | |
| ID: 129663966 | ReSE screen-validated silencer GRCh37_chr17:7481957-7482145 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7578639..7578827) | | |
| ID: 129390831 | MPRA-validated peak2713 silencer [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7619718..7619918) | | |
| ID: 127885668 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7492556-7493130 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7589238..7589812) | | |
| ID: 127885667 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7487743-7488615 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7584425..7585297) | | |
| ID: 127885666 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7486868-7487742 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7583550..7584424) | | |
| ID: 127885665 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7485994-7486867 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7582676..7583550) | | |
| ID: 124904134 | uncharacterized LOC124904134 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7611181..7611273) | | |
| ID: 103482525 | tRNA-undetermined (NNN) 6-1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7621139..7621207) | tRNA-Und-NNN-6-1 | |
| ID: 100996842 | MPDU1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7581967..7584092, complement) | | |
| ID: 100533955 | SENP3-EIF4A1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7561992..7579006) | | |
| ID: 26781 | small nucleolar RNA, H/ACA box 67 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7577955..7578091) | RNU67, U67 | |
| ID: 9526 | mannose-P-dolichol utilization defect 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7583647..7588212) | CDGIF, HBEBP2BPA, Lec35, My008, PP3958, PQLC5, SL15, SLC66A5 | 604041 |
| ID: 9513 | FMR1 autosomal homolog 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7591230..7614897, complement) | FMR1L2P, FXR2 | 605339 |
| ID: 6665 | SRY-box transcription factor 15 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7588178..7590094, complement) | SOX20, SOX26, SOX27 | 601297 |
| ID: 6462 | sex hormone binding globulin [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7614064..7633372) | ABP, SBP, TEBG | 182205 |
| ID: 1973 | eukaryotic translation initiation factor 4A1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7572825..7579006) | DDX2A, EIF-4A, EIF4A, eIF-4A-I, eIF4A-I | 602641 |