| ID: 100506747 | MGAT4 family member F, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (202986452..203007265, complement) | | |
| ID: 100130996 | YPEL5 pseudogene 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (182182038..182183133, complement) | | |
| ID: 646981 | PTPN2 pseudogene 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (178746344..178747830, complement) | PTPN2P, PTPTP1 | |
| ID: 440712 | regulator of hemoglobinization and erythroid cell expansion [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (206053173..206102449) | C1orf186 | 616088 |
| ID: 403314 | apolipoprotein B mRNA editing enzyme catalytic polypeptide like 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (183646275..183653316, complement) | C1orf169 | 609908 |
| ID: 400798 | chromosome 1 putative open reading frame 220 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (178542796..178548889) | | |
| ID: 400793 | chromosome 1 open reading frame 226 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (162378841..162386812) | | |
| ID: 388730 | transmembrane protein 81 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (205083129..205084460, complement) | HC3107, KVLA2788, UNQ2788 | |
| ID: 388722 | chromosome 1 open reading frame 53 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (197902630..197907362) | | |
| ID: 388719 | long intergenic non-protein coding RNA 272 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (182407621..182414813) | C1orf120, NCRNA00272 | |
| ID: 387597 | immunoglobulin like domain containing receptor 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166908187..166975540, complement) | C1orf32, dJ782G3.1 | 618081 |
| ID: 375035 | SFT2 domain containing 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (168226004..168253021) | UNQ512, dJ747L4.C1.2 | |
| ID: 360023 | zinc finger and BTB domain containing 41 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (197153682..197201293, complement) | FRBZ1, ZNF924 | |
| ID: 353299 | regulator of G protein signaling like 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (182447877..182560597) | RGSL, RGSL2 | 611012 |
| ID: 343450 | potassium sodium-activated channel subfamily T member 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (196225779..196608440, complement) | DEE57, EIEE57, KCa4.2, KNa1.2, SLICK, SLO2.1 | 610044 |
| ID: 339521 | CCNQ pseudogene 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (200213532..200214762) | FAM58B, FAM58BP | |
| ID: 339512 | coiled-coil domain containing 190 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (162851020..162868833, complement) | C1orf110 | |
| ID: 339479 | BMP/retinoic acid inducible neural specific 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (190097658..190477864, complement) | DBCCR1L, DBCCR1L1, FAM5C | 618390 |
| ID: 339476 | endogenous retrovirus group MER61 member 1 [Homo sapiens (human)] | | C1orf99, TP53LC07 | |
| ID: 339416 | ankyrin repeat domain 45 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (173608336..173715185, complement) | CT117 | 618712 |