| ID: 127822450 | H3K27ac hESC enhancer GRCh37_chr11:102962627-102963244 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103091898..103092515) | | |
| ID: 127822449 | NANOG hESC enhancer GRCh37_chr11:102852196-102852783 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (102981467..102982054) | | |
| ID: 126861318 | BRD4-independent group 4 enhancer GRCh37_chr11:102825894-102827093 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (102955165..102956364) | | |
| ID: 124625829 | H3K27ac hESC enhancer GRCh37_chr11:102962009-102962626 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103091280..103091897) | | |
| ID: 106481747 | RNA, U7 small nuclear 159 pseudogene [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (102903892..102903953, complement) | | |
| ID: 100288111 | bolA family member 3 pseudogene 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (102880484..102881038) | | |
| ID: 100271428 | ribosomal protein L21 pseudogene 96 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103045203..103045739) | RPL21_41_1169 | |
| ID: 84259 | defective in cullin neddylation 1 domain containing 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103050686..103092160, complement) | DCNL5, SCCRO5 | 616522 |
| ID: 4322 | matrix metallopeptidase 13 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (102942995..102955732, complement) | CLG3, MANDP1, MDST, MMP-13 | 600108 |