| ID: 8669 | eukaryotic translation initiation factor 3 subunit J [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (44537147..44562803) | EIF3S1, eIF3-alpha, eIF3-p35 | 603910 |
| ID: 8939 | far upstream element binding protein 3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130579577..130638352) | FBP3 | 603536 |
| ID: 10771 | zinc finger MYND-type containing 11 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (130088..254637) | BRAM1, BS69, MRD30 | 608668 |
| ID: 5531 | protein phosphatase 4 catalytic subunit [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30075994..30085376) | PP-X, PP4, PP4C, PPH3, PPP4, PPX | 602035 |
| ID: 90809 | phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20457681..20461434, complement) | C14orf9, TMEM55B | 609865 |
| ID: 6714 | SRC proto-oncogene, non-receptor tyrosine kinase [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (37344699..37406050) | ASV1, THC6, c-SRC, p60-Src, SRC | 190090 |
| ID: 8816 | DDB1 and CUL4 associated factor 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69050881..69153197, complement) | BCRG2, BCRP2, D14S1461E, WDR22 | 603812 |
| ID: 112398 | egl-9 family hypoxia inducible factor 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40799191..40808434) | EIT-6, EIT6, HIF-PH1, HIFPH1, HPH-1, HPH-3, PHD1 | 606424 |
| ID: 23186 | REST corepressor 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102592649..102730561) | COREST, RCOR | 607675 |
| ID: 6709 | spectrin alpha, non-erythrocytic 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128552587..128633662) | DEE5, DEVEP, EIEE5, HMN11, HMND11, NEAS, SPG91, SPTA2 | 182810 |
| ID: 54904 | nuclear receptor binding SET domain protein 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38269704..38382271, complement) | KMT3F, KMT3G, WHISTLE, WHSC1L1, pp14328 | 607083 |
| ID: 158405 | KIAA1958 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (112486827..112669397) | | 617390 |
| ID: 121274 | zinc finger protein 641 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48334587..48351246, complement) | | 613906 |
| ID: 84333 | polycomb group ring finger 5 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (91156219..91284337) | RNF159 | 617407 |
| ID: 55225 | ribonucleoprotein, PTB binding 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (64745075..64833232) | | 609953 |