ID: 129662875 | ReSE screen-validated silencer GRCh37_chr11:17550891-17551094 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17529344..17529547) | | |
ID: 127820567 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:17742579-17743090 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17721032..17721543) | | |
ID: 127820566 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:17742067-17742578 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17720520..17721031) | | |
ID: 127820565 | H3K4me1 hESC enhancer GRCh37_chr11:17736199-17736699 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17714652..17715152) | | |
ID: 127820564 | H3K4me1 hESC enhancer GRCh37_chr11:17672009-17672509 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17650462..17650962) | | |
ID: 127820563 | H3K4me1 hESC enhancer GRCh37_chr11:17667297-17667797 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17645750..17646250) | | |
ID: 127820562 | H3K4me1 hESC enhancer GRCh37_chr11:17666796-17667296 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17645249..17645749) | | |
ID: 127820561 | H3K4me1 hESC enhancer GRCh37_chr11:17626113-17626614 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17604566..17605067) | | |
ID: 127820560 | H3K4me1 hESC enhancer GRCh37_chr11:17623679-17624178 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17602132..17602631) | | |
ID: 127820559 | H3K4me1 hESC enhancer GRCh37_chr11:17517053-17517553 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17495506..17496006) | | |
ID: 127820558 | H3K4me1 hESC enhancer GRCh37_chr11:17516552-17517052 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17495005..17495505) | | |
ID: 127820557 | H3K4me1 hESC enhancer GRCh37_chr11:17514781-17515280 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17493234..17493733) | | |
ID: 127820556 | H3K4me1 hESC enhancer GRCh37_chr11:17497048-17497604 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17475501..17476057) | | |
ID: 124902641 | uncharacterized LOC124902641 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17476651..17492365) | | |
ID: 112067714 | Sharpr-MPRA regulatory region 13094 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17704022..17704316) | | |
ID: 112067713 | Sharpr-MPRA regulatory region 4357 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17699542..17699836) | | |
ID: 102723330 | long intergenic non-protein coding RNA 2729 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17695267..17696939, complement) | | |
ID: 100422598 | SDHC pseudogene 4 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17435023..17436206, complement) | | |
ID: 340990 | otogelin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17547259..17646044) | DFNB18B, MLEMP, OTGN | 604487 |
ID: 10083 | USH1 protein network component harmonin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17493900..17544416, complement) | AIE-75, DFNB18, DFNB18A, NY-CO-37, NY-CO-38, PDZ-45, PDZ-73, PDZ-73/NY-CO-38, PDZ73, PDZD7C, ush1cpst | 605242 |