Variant report

Variant	rs16936126
Chromosome Location	chr11:19111668-19111669
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10500838	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10500840	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10833055	0.94[YRI][hapmap]
rs16924998	1.00[AMR][1000 genomes]
rs16936120	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936124	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936127	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936137	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936146	0.86[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41420346	0.82[AFR][1000 genomes]
rs59309964	1.00[AMR][1000 genomes]
rs60139631	1.00[AMR][1000 genomes]
rs61056306	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040805	chr11:19037871-19892803	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv540957	chr11:19037871-19892803	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv3457408	chr11:19111213-19111759	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3457397	chr11:19111269-19111725	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3457385	chr11:19111278-19111720	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3457419	chr11:19111284-19111683	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3457374	chr11:19111337-19111673	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3457430	chr11:19111351-19111669	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:19104800-19111800	Weak transcription	Esophagus	oesophagus
2	chr11:19108200-19113400	Enhancers	HUVEC	blood vessel
3	chr11:19109800-19111800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:19110000-19112000	Weak transcription	NH-A	brain
5	chr11:19110000-19115400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr11:19110400-19112800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:19110600-19112000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:19110800-19112000	Enhancers	NHEK	skin

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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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