Variant report

Variant	rs56061726
Chromosome Location	chr11:26730617-26730618
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16916148	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs16916156	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4370890	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs60517765	0.89[AMR][1000 genomes]
rs61073671	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7925046	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044544	chr11:26506962-26967285	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv916187	chr11:26576875-27328603	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26721200-26741200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:26726000-26733800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:26726400-26732200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr11:26727000-26734200	Weak transcription	Fetal Intestine Small	intestine
5	chr11:26730400-26731000	Enhancers	Fetal Lung	lung
6	chr11:26730400-26731400	Enhancers	Colon Smooth Muscle	Colon
7	chr11:26730400-26731400	Enhancers	Rectal Smooth Muscle	rectum
8	chr11:26730400-26731600	Enhancers	Fetal Heart	heart
9	chr11:26730400-26732200	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr11:26730600-26730800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:26730600-26730800	Weak transcription	Fetal Intestine Large	intestine
12	chr11:26730600-26731400	Enhancers	Fetal Stomach	stomach

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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