| ID: 115830330 | LONRF2 pseudogene 5 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (13704853..13705518) | | |
| ID: 112268283 | uncharacterized LOC112268283 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (13723504..13753242) | | |
| ID: 111216285 | long intergenic non-protein coding RNA 2573 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (20256862..20258685, complement) | | |
| ID: 110806272 | BTG3 antisense RNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (17611686..17614114) | ASBEL | |
| ID: 110091776 | ankyrin repeat domain 18B pseudogene [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (13909448..13933879, complement) | | |
| ID: 109617014 | small nucleolar RNA, C/D box 74B [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (16284696..16284768, complement) | | |
| ID: 107987295 | adipocyte associated metabolic related lncRNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14816838..14918668, complement) | ASMER-1, LINC02246 | |
| ID: 107985516 | uncharacterized LOC107985516 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (24987065..24993055, complement) | | |
| ID: 107985512 | uncharacterized LOC107985512 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (23413893..23423676, complement) | | |
| ID: 107985511 | uncharacterized LOC107985511 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (17191574..17271161) | | |
| ID: 107985508 | uncharacterized LOC107985508 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (22209920..22403096) | | |
| ID: 107985494 | uncharacterized LOC107985494 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (22555182..22560576) | | |
| ID: 107985490 | uncharacterized LOC107985490 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (19128637..19134175) | | |
| ID: 107985483 | uncharacterized LOC107985483 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (15105119..15138607, complement) | | |
| ID: 107985482 | uncharacterized LOC107985482 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (13705881..13713853) | | |
| ID: 107985474 | uncharacterized LOC107985474 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (26458259..26471698) | | |
| ID: 107063541 | cytochrome P450 family 2 subfamily C member 63, pseudogene [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (25446235..25446381, complement) | | |
| ID: 106481961 | RNA, U2 small nuclear 55, pseudogene [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (23281736..23281909, complement) | | |
| ID: 106481951 | RNA, U6 small nuclear 1326, pseudogene [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (15614283..15614389) | | |
| ID: 106481739 | FSHD region gene 2 family member M, pseudogene [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14019060..14020725, complement) | | |