ID: 132089922 | Neanderthal introgressed variant-containing enhancer experimental_20715 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22028525..22028694) | | |
ID: 132089921 | Neanderthal introgressed variant-containing enhancer experimental_20562 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21799496..21799665) | | |
ID: 132089920 | Neanderthal introgressed variant-containing enhancer experimental_20507 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21762338..21762507) | | |
ID: 132089919 | Neanderthal introgressed variant-containing enhancer experimental_20487 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21756674..21756843) | | |
ID: 132089918 | Neanderthal introgressed variant-containing enhancer experimental_20421 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21553685..21553854) | | |
ID: 132089917 | Neanderthal introgressed variant-containing enhancer experimental_20387 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21531989..21532158) | | |
ID: 132089916 | Neanderthal introgressed variant-containing enhancer experimental_20249 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21356563..21356732) | | |
ID: 132089915 | Neanderthal introgressed variant-containing enhancer experimental_20242 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21332815..21332984) | | |
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: 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: 127820635 | OCT4-NANOG hESC enhancer GRCh37_chr11:22086967-22087603 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22065421..22066057) | | |
ID: 127820634 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:22042648-22043247 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22021102..22021701) | | |
ID: 127820633 | OCT4-NANOG hESC enhancer GRCh37_chr11:21882755-21883281 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21861209..21861735) | | |
ID: 127820632 | H3K27ac hESC enhancer GRCh37_chr11:21311115-21311614 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21289569..21290068) | | |
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: 126861160 | MED14-independent group 3 enhancer GRCh37_chr11:21831599-21832798 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (21810053..21811252) | | |