| ID: 127894597 | NANOG hESC enhancer GRCh37_chr21:36965152-36965707 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35592854..35593409) | | |
| ID: 127894596 | NANOG hESC enhancer GRCh37_chr21:36880486-36881006 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35508188..35508708) | | |
| ID: 127894595 | OCT4-NANOG hESC enhancer GRCh37_chr21:36878653-36879242 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35506355..35506944) | | |
| ID: 127894594 | NANOG hESC enhancer GRCh37_chr21:36743463-36743964 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35371165..35371666) | | |
| ID: 127894593 | H3K4me1 hESC enhancer GRCh37_chr21:36646465-36646966 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35274167..35274668) | | |
| ID: 126653358 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr21:37006276-37007475 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35633978..35635177) | | |
| ID: 126653357 | MED14-independent group 3 enhancer GRCh37_chr21:36897177-36898376 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35524879..35526078) | | |
| ID: 125418069 | NANOG hESC enhancer GRCh37_chr21:36786783-36787398 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35414485..35415100) | | |
| ID: 125418068 | Sharpr-MPRA regulatory region 5568 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35400491..35400785) | | |
| ID: 125418067 | Sharpr-MPRA regulatory region 14404 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35377531..35377825) | | |
| ID: 100506403 | uncharacterized LOC100506403 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35372507..35580764, complement) | | |
| ID: 768219 | microRNA 802 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35720715..35720808) | MIRN802, hsa-mir-802 | 616090 |
| ID: 80215 | RUNX1 intronic transcript 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35037925..35039426, complement) | C21orf96 | |
| ID: 54026 | ribosomal protein L34 pseudogene 3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35472076..35472455, complement) | | |
| ID: 54025 | ribosomal protein S20 pseudogene 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (35724708..35725166, complement) | RPS20P, RPS20_16_1728 | |
| ID: 861 | RUNX family transcription factor 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34787801..35049302, complement) | AML1, AML1-EVI-1, AMLCR1, CBF2alpha, CBFA2, EVI-1, PEBP2aB, PEBP2alpha | 151385 |