| ID: 128966692 | putative uncharacterized protein LOC388882 [Homo sapiens (human)] | | | |
| ID: 128966596 | putative uncharacterized protein LOC388882 [Homo sapiens (human)] | | | |
| ID: 127895261 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:18934751-18935496 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18947238..18947983) | | |
| ID: 127895260 | H3K4me1 hESC enhancer GRCh37_chr22:18897340-18898042 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18909827..18910529) | | |
| ID: 127895259 | H3K4me1 hESC enhancer GRCh37_chr22:18896637-18897339 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18909124..18909826) | | |
| ID: 127895258 | H3K4me1 hESC enhancer GRCh37_chr22:18895933-18896636 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18908420..18909123) | | |
| ID: 127895257 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:18893839-18894376 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18906326..18906863) | | |
| ID: 127895256 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:18893301-18893838 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18905788..18906325) | | |
| ID: 127895255 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:18892762-18893300 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18905249..18905787) | | |
| ID: 127895254 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:18891787-18892644 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18904274..18905131) | | |
| ID: 127895253 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:18890927-18891786 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18903414..18904273) | | |
| ID: 127895252 | OCT4 hESC enhancer GRCh37_chr22:18883553-18884054 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18896040..18896541) | | |
| ID: 122455341 | uncharacterized LOC122455341 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18937375..18947693) | | |
| ID: 106660608 | human-specific endogenous retroviral insert PRODH enhancer [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18936275..18939737) | hsERV_PRODH | |
| ID: 102725072 | POM121 transmembrane nucleoporin like 15, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18846286..18861064) | | |
| ID: 100996432 | family with sequence similarity 230 member F [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18865042..18896764, complement) | LINC01663 | |
| ID: 100133163 | BCR pseudogene 7 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18852284..18858643, complement) | | |
| ID: 8214 | DiGeorge syndrome critical region gene 6 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18906223..18912088) | | 601279 |
| ID: 5625 | proline dehydrogenase 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18912781..18936553, complement) | HSPOX2, PIG6, POX1, PRODH2, TP53I6, PRODH | 606810 |