ID: 132090809 | Neanderthal introgressed variant-containing enhancer experimental_12564 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43864764..43864933) | | |
ID: 132090808 | Neanderthal introgressed variant-containing enhancer experimental_12499 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43842316..43842485) | | |
ID: 132089778 | Neanderthal introgressed variant-containing enhancer experimental_12586 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43875696..43875865) | | |
ID: 129662683 | ReSE screen-validated silencer GRCh37_chr10:44372279-44372466 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43876831..43877018) | | |
ID: 129390166 | MPRA-validated peak936 silencer [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43816567..43816767) | | |
ID: 127817832 | H3K4me1 hESC enhancer GRCh37_chr10:44358949-44359449 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43863501..43864001) | | |
ID: 127817831 | H3K4me1 hESC enhancer GRCh37_chr10:44358448-44358948 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43863000..43863500) | | |
ID: 127817830 | H3K4me1 hESC enhancer GRCh37_chr10:44249197-44249908 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43753749..43754460) | | |
ID: 124403946 | Sharpr-MPRA regulatory region 2960 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43867161..43867455) | | |
ID: 106481670 | elongin C pseudogene 30 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43741275..43742421, complement) | TCEB1P30 | |
ID: 105378275 | uncharacterized LOC105378275 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43778946..43818744) | | |
ID: 102724264 | long intergenic non-protein coding RNA 2658 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43777562..43778902, complement) | | |
ID: 100506835 | long intergenic non-protein coding RNA 840 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43859411..43895433) | | |
ID: 414260 | long intergenic non-protein coding RNA 619 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43845306..43850622) | C10orf136, bA168P8.1 | |
ID: 10151 | heterogeneous nuclear ribonucleoprotein A3 pseudogene 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43787412..43790417, complement) | D10S102, FBRNP, HNRPA3, HNRPA3P1 | |