| ID: 130066949 | ATAC-STARR-seq lymphoblastoid silent region 13451 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19036019..19036188) | | |
| ID: 129664770 | ReSE screen-validated silencer GRCh37_chr22:18985578-18985746 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18998065..18998233) | | |
| ID: 127895266 | H3K4me1 hESC enhancer GRCh37_chr22:19024185-19024805 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19036672..19037292) | | |
| ID: 127895265 | H3K4me1 hESC enhancer GRCh37_chr22:19007165-19007664 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19019652..19020151) | | |
| ID: 127895264 | H3K4me1 hESC enhancer GRCh37_chr22:19005353-19005854 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19017840..19018341) | | |
| ID: 127895263 | H3K4me1 hESC enhancer GRCh37_chr22:18957062-18957893 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18969549..18970380) | | |
| ID: 127895262 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:18945292-18945809 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18957779..18958296) | | |
| ID: 127895261 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:18934751-18935496 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18947238..18947983) | | |
| ID: 122455341 | uncharacterized LOC122455341 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18937375..18947693) | | |
| ID: 117134596 | family with sequence similarity 246 member C (gene/pseudogene) [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19029524..19030221) | | |
| ID: 106660608 | human-specific endogenous retroviral insert PRODH enhancer [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18936275..18939737) | hsERV_PRODH | |
| ID: 100996435 | CA15 pseudogene 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19031528..19034922, complement) | | |
| ID: 26220 | DiGeorge syndrome critical region gene 5 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18970468..19031242) | DGCR10, DGCR9, DGS-A, DGS-B, LINC00037, NCRNA00037, POM121L5P, RIP | 618040 |
| ID: 25786 | DiGeorge syndrome critical region gene 11 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19046162..19048375, complement) | DGS-D | |
| ID: 9993 | DiGeorge syndrome critical region gene 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19036286..19122412, complement) | DGS-C, IDD, LAN, SEZ-12 | 600594 |
| ID: 5625 | proline dehydrogenase 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (18912781..18936553, complement) | HSPOX2, PIG6, POX1, PRODH2, TP53I6, PRODH | 606810 |