| ID: 6871 | transcriptional adaptor 2A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37406886..37479725) | ADA2, ADA2A, KL04P, TADA2L, hADA2 | 602276 |
| ID: 31 | acetyl-CoA carboxylase alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37084992..37406836, complement) | ACACD, ACACalpha, ACC, ACC1, ACCA, ACCalpha, Acac1, hACC1, ACACA | 200350 |
| ID: 51167 | cytochrome b5 reductase 4 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83859689..83967423) | NCB5OR, cb5/cb5R, dJ676J13.1 | 608343 |
| ID: 79736 | transcription elongation factor, mitochondrial [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30898986..30906238, complement) | C17orf42, COXPD58 | 616422 |
| ID: 3275 | protein arginine methyltransferase 2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46635674..46665124) | HRMT1L1 | 601961 |
| ID: 427 | N-acylsphingosine amidohydrolase 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (18055992..18084961, complement) | AC, ACDase, ASAH, PHP, PHP32, SMAPME | 613468 |
| ID: 4864 | NPC intracellular cholesterol transporter 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (23506184..23586506, complement) | NPC, POGZ, SLC65A1 | 607623 |
| ID: 79230 | zinc finger protein 557 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7069703..7087968) | | |
| ID: 2618 | phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33503931..33542893, complement) | AIRS, GARSF, PAIS, PGFT, PRGS, GART | 138440 |
| ID: 90799 | centrosomal protein 95 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64506762..64537946) | CCDC45 | |
| ID: 342892 | zinc finger protein 850 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (36743480..36772807, complement) | ZNF850P | |
| ID: 23341 | DnaJ heat shock protein family (Hsp40) member C16 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (15526848..15571733) | ERdj8 | 619973 |
| ID: 8677 | syntaxin 10 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13144058..13150375, complement) | SYN10, hsyn10 | 603765 |
| ID: 1340 | cytochrome c oxidase subunit 6B1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35648323..35658782) | COX6B, COXG, COXVIb1, MC4DN7 | 124089 |
| ID: 64743 | WD repeat domain 13 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48597492..48608869) | MG21 | 300512 |
| ID: 55850 | unconventional SNARE in the ER 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17215357..17219829) | D12, MDS032, P31, SLT1 | 610675 |
| ID: 79031 | phosducin like 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100562993..100576739) | HTPHLP, PHLP2A, PHLP3, VIAF, VIAF1 | 611678 |