ID: 127818770 | NANOG hESC enhancer GRCh37_chr10:94110043-94110561 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92350286..92350804) | | |
ID: 127818769 | H3K4me1 hESC enhancer GRCh37_chr10:94107981-94108480 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92348224..92348723) | | |
ID: 127818768 | H3K27ac hESC enhancer GRCh37_chr10:94072769-94073270 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92313012..92313513) | | |
ID: 127818767 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:94066611-94067322 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92306854..92307565) | | |
ID: 127818766 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:94065899-94066610 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92306142..92306853) | | |
ID: 127818765 | H3K27ac hESC enhancer GRCh37_chr10:94051286-94051864 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92291529..92292107) | | |
ID: 124902484 | uncharacterized LOC124902484 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92423010..92427623) | | |
ID: 124902483 | uncharacterized LOC124902483 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92241189..92244026) | | |
ID: 106480315 | RNY3 pseudogene 12 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92334468..92334561) | | |
ID: 100507674 | MARK2 pseudogene 9 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92418661..92419606) | | |
ID: 100289102 | eukaryotic translation initiation factor 4A1 pseudogene 8 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92136861..92138515) | | |
ID: 414200 | NHP2 ribonucleoprotein pseudogene 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92216292..92217043) | NOLA2P1, bA360G10.4 | |
ID: 54708 | membrane associated ring-CH-type finger 5 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92291167..92353964) | MARCH-V, MARCH5, MITOL, RNF153 | 610637 |
ID: 22849 | cytoplasmic polyadenylation element binding protein 3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92046692..92291233, complement) | | 610606 |