| ID: 127405851 | H3K4me1 hESC enhancer GRCh37_chr6:32041114-32041614 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32073337..32073837) | | |
| ID: 127405846 | H3K4me1 hESC enhancer GRCh37_chr6:31915103-31915602 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31947326..31947825) | | |
| ID: 127405845 | H3K27ac hESC enhancer GRCh37_chr6:31865398-31865992 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31897621..31898215) | | |
| ID: 127405844 | H3K4me1 hESC enhancer GRCh37_chr6:31864618-31865314 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31896841..31897537) | | |
| ID: 127405843 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31838055-31838988 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31870278..31871211) | | |
| ID: 127405842 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31832029-31832653 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31864252..31864876) | | |
| ID: 107986588 | EHMT2 and SLC44A4 antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31877808..31884204) | | |
| ID: 106478999 | RNA, 5S ribosomal pseudogene 206 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32078508..32078628, complement) | RN5S206 | |
| ID: 102060414 | C2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31934474..31941724, complement) | | |
| ID: 221527 | zinc finger and BTB domain containing 12 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31899613..31902086, complement) | Bat9, C6orf46, D6S59E, G10, NG35 | |
| ID: 80736 | solute carrier family 44 member 4 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31863192..31878997, complement) | C6orf29, CTL4, DFNA72, NG22, TPPT, hTPPT1 | 606107 |
| ID: 10919 | euchromatic histone lysine methyltransferase 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31879759..31897698, complement) | BAT8, C6orf30, G9A, GAT8, KMT1C, NG36 | 604599 |
| ID: 7148 | tenascin XB [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32041153..32109338, complement) | EDS3, EDSCLL, EDSCLL1, HXBL, TENX, TN-X, TNX1, TNXB2, TNXBS, VUR8, XB, XBS, TNXB | 600985 |
| ID: 717 | complement C2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31897783..31945672) | ARMD14, CO2 | 613927 |
| ID: 629 | complement factor B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31946095..31952084) | AHUS4, ARMD14, BF, BFD, CFABD, FB, FBI12, GBG, H2-Bf, PBF2, CFB | 138470 |