| ID: 132089914 | Neanderthal introgressed variant-containing enhancer experimental_20084 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20605327..20605496) | | |
| ID: 132089913 | Neanderthal introgressed variant-containing enhancer experimental_20054 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20593406..20593575) | | |
| ID: 132089912 | Neanderthal introgressed variant-containing enhancer experimental_20020 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20561146..20561315) | | |
| ID: 129662884 | ReSE screen-validated silencer GRCh37_chr11:20787638-20787848 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20766092..20766302) | | |
| ID: 129662883 | ReSE screen-validated silencer GRCh37_chr11:20631780-20631977 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20610234..20610479) | | |
| ID: 127820631 | OCT4-NANOG hESC enhancer GRCh37_chr11:20987919-20988485 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20966373..20966939) | | |
| ID: 127820630 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:20902693-20903205 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20881147..20881659) | | |
| ID: 127820629 | H3K4me1 hESC enhancer GRCh37_chr11:20643011-20643512 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20621465..20621966) | | |
| ID: 124421507 | Sharpr-MPRA regulatory region 9738 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20605663..20606011) | | |
| ID: 105376585 | uncharacterized LOC105376585 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20880631..20926796, complement) | | |
| ID: 105376584 | uncharacterized LOC105376584 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20560068..20572998, complement) | | |
| ID: 100873599 | RNA, 5S ribosomal pseudogene 336 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21000881..21000997, complement) | RN5S336 | |
| ID: 100506595 | high mobility group box 1 pseudogene 40 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20574132..20575359) | | |
| ID: 9152 | solute carrier family 6 member 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20599608..20659285) | GLYT-2, GLYT2, HKPX3, NET1 | 604159 |
| ID: 4745 | neural EGFL like 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20669551..21575686) | IDH3GL, NRP1 | 602319 |