| ID: 127404341 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:150974668-150975189 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151595107..151595628) | | |
| ID: 127404340 | H3K4me1 hESC enhancer GRCh37_chr5:150950930-150951442 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151571369..151571881) | | |
| ID: 127404339 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:150877439-150878100 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151497878..151498539) | | |
| ID: 127404338 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:150875552-150876101 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151495991..151496540) | | |
| ID: 127404336 | NANOG-H3K4me1 hESC enhancers GRCh37_chr5:150804400-150804900 and GRCh37_chr5:150804901-150805401 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151424839..151425840) | | |
| ID: 127404335 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:150767117-150768055 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151387556..151388494) | | |
| ID: 127404334 | H3K4me1 hESC enhancer GRCh37_chr5:150726633-150727546 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151347072..151347985) | | |
| ID: 105378234 | uncharacterized LOC105378234 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151352399..151436938, complement) | | |
| ID: 102465246 | microRNA 6499 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151522087..151522148, complement) | hsa-mir-6499, mir-6499 | |
| ID: 100873459 | RNA, 5S ribosomal pseudogene 197 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151477459..151477577, complement) | RN5S197 | |
| ID: 100462840 | ATPase H+ transporting V1 subunit G1 pseudogene 5 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151319425..151319778) | | |
| ID: 100420127 | mediator complex subunit 13 pseudogene [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151377999..151378709, complement) | | |
| ID: 100419720 | RUN domain containing 1 pseudogene [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151380339..151382580) | | |
| ID: 285641 | solute carrier family 36 member 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151276358..151303766, complement) | PAT3, TRAMD2, tramdorin2 | 608332 |
| ID: 206358 | solute carrier family 36 member 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151344596..151556085) | Dct1, LYAAT1, PAT1, TRAMD3 | 606561 |
| ID: 153201 | solute carrier family 36 member 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151314972..151347559, complement) | PAT2, TRAMD1 | 608331 |
| ID: 2760 | ganglioside GM2 activator [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151253185..151270440) | GM2-APP, SAP-3, GM2A | 613109 |
| ID: 2196 | FAT atypical cadherin 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151504092..151594819, complement) | CDHF8, CDHR9, HFAT2, MEGF1, SCA45 | 604269 |