ID: 127822025 | H3K4me1 hESC enhancer GRCh37_chr11:72493384-72494086 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72782339..72783041) | | |
ID: 127822024 | H3K4me1 hESC enhancer GRCh37_chr11:72485809-72486308 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72774764..72775263) | | |
ID: 127822023 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:72453754-72454530 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72742709..72743485) | | |
ID: 127822022 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:72452199-72452976 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72741154..72741931) | | |
ID: 127822021 | H3K4me1 hESC enhancer GRCh37_chr11:72428974-72429474 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72717929..72718429) | | |
ID: 127822020 | H3K4me1 hESC enhancer GRCh37_chr11:72428169-72428669 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72717124..72717624) | | |
ID: 127822019 | H3K4me1 hESC enhancer GRCh37_chr11:72424849-72425428 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72713804..72714383) | | |
ID: 127822018 | H3K4me1 hESC enhancer GRCh37_chr11:72423687-72424267 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72712642..72713222) | | |
ID: 127822017 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:72420686-72421388 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72709641..72710343) | | |
ID: 127822016 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:72417010-72417596 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72705965..72706551) | | |
ID: 127822015 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:72415096-72415932 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72704051..72704887) | | |
ID: 127822014 | H3K4me1 hESC enhancer GRCh37_chr11:72395779-72396338 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72684734..72685293) | | |
ID: 127822013 | H3K4me1 hESC enhancer GRCh37_chr11:72391485-72392310 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72680440..72681265) | | |
ID: 127822012 | H3K4me1 hESC enhancer GRCh37_chr11:72386690-72387190 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72675646..72676146) | | |
ID: 100506020 | ARAP1 antisense RNA 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72700474..72705607) | | |
ID: 100271549 | ribosomal protein S12 pseudogene 20 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72708186..72708565) | RPS12_10_1153 | |
ID: 116985 | ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72685069..72752408, complement) | CENTD2, cnt-d2 | 606646 |
ID: 10809 | StAR related lipid transfer domain containing 10 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72754729..72794047, complement) | CGI-52, NY-CO-28, PCTP2, SDCCAG28 | 617382 |