ID: 127818133 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:70287929-70288614 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68528172..68528857) | | |
ID: 127818132 | NANOG-H3K27ac hESC enhancer GRCh37_chr10:70285872-70286556 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68526115..68526799) | | |
ID: 127818131 | OCT4-NANOG hESC enhancer GRCh37_chr10:70255753-70256326 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68495969..68496569) | | |
ID: 111982863 | Sharpr-MPRA regulatory region 5966 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68527220..68527666) | | |
ID: 100873585 | RNA, 5S ribosomal pseudogene 319 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68461407..68461525) | RN5S319 | |
ID: 100271471 | ribosomal protein L26 pseudogene 27 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68499490..68500009) | RPL26_15_1055 | |
ID: 100131788 | ribosomal protein L26 pseudogene 29 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68424560..68424997) | RPL26_14_1054 | |
ID: 645203 | transmembrane protein 14D, pseudogene [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68544026..68544940, complement) | TMEM14D, bA524O24.3 | |
ID: 8034 | solute carrier family 25 member 16 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68477998..68527523, complement) | D10S105E, GDA, GDC, HGT.1, ML7, hGP, hML7 | 139080 |
ID: 1763 | DNA replication helicase/nuclease 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68414064..68472521, complement) | DNA2L, hDNA2 | 601810 |