ID: 130067229 | ATAC-STARR-seq lymphoblastoid silent region 13620 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30969536..30969785) | | |
ID: 130067228 | ATAC-STARR-seq lymphoblastoid active region 18847 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30969176..30969505) | | |
ID: 130067227 | ATAC-STARR-seq lymphoblastoid active region 18846 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30903241..30903340) | | |
ID: 129664836 | ReSE screen-validated silencer GRCh37_chr22:31335586-31335801 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30939599..30939814) | | |
ID: 129391277 | MPRA-validated peak4481 silencer [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (31003110..31003310) | | |
ID: 127895886 | H3K4me1 hESC enhancer GRCh37_chr22:31440503-31441072 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (31044517..31045086) | | |
ID: 127895885 | H3K4me1 hESC enhancer GRCh37_chr22:31439932-31440502 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (31043946..31044516) | | |
ID: 127895884 | H3K4me1 hESC enhancer GRCh37_chr22:31289553-31290128 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30893566..30894141) | | |
ID: 127895883 | H3K4me1 hESC enhancer GRCh37_chr22:31288977-31289552 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30892990..30893565) | | |
ID: 127895882 | NANOG-H3K4me1 hESC enhancer GRCh37_chr22:31281999-31282696 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30886012..30886709) | | |
ID: 127895881 | H3K4me1 hESC enhancer GRCh37_chr22:31274410-31275151 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30878423..30879164) | | |
ID: 127895880 | H3K4me1 hESC enhancer GRCh37_chr22:31273667-31274409 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30877680..30878422) | | |
ID: 127895879 | H3K4me1 hESC enhancer GRCh37_chr22:31268713-31269213 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30872726..30873226) | | |
ID: 107985544 | uncharacterized LOC107985544 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30886056..30921779, complement) | | |
ID: 107275225 | origin of replication in OSBP2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30883152..30883435) | | |
ID: 106479453 | RNA, 7SL, cytoplasmic 633, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (31059989..31060285) | | |
ID: 105372994 | uncharacterized LOC105372994 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30872890..30877375, complement) | | |
ID: 100421545 | eukaryotic translation initiation factor 4H pseudogene 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30902153..30902972) | | |
ID: 150291 | MORC2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30922308..30926654) | C22orf27, NCRNA00325 | |
ID: 55000 | taurine up-regulated 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30969265..30979395) | LINC00080, NCRNA00080, TI-227H | 614971 |