Variant report

Variant	rs7926101
Chromosome Location	chr11:18713180-18713181
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs16935626	0.85[AMR][1000 genomes]
rs35096313	0.82[AFR][1000 genomes]
rs58088308	0.85[AMR][1000 genomes]
rs58298594	0.83[AMR][1000 genomes]
rs59616087	0.85[AMR][1000 genomes]
rs59965930	1.00[AMR][1000 genomes]
rs60701947	1.00[AMR][1000 genomes]
rs7116232	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7118958	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73426408	1.00[AMR][1000 genomes]
rs73426427	0.85[AMR][1000 genomes]
rs73426461	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73426477	1.00[AMR][1000 genomes]
rs7930849	0.85[AMR][1000 genomes]
rs7947182	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553633	chr11:18311701-19058451	Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv1046886	chr11:18547568-18781448	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	nsv540956	chr11:18547568-18781448	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
4	nsv983163	chr11:18702181-18736146	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3384506	chr11:18703609-18713322	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18687000-18719800	Weak transcription	Ovary	ovary
2	chr11:18703400-18719800	Weak transcription	Right Atrium	heart
3	chr11:18712600-18713600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:18712600-18713800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:18712600-18714400	Enhancers	K562	blood
6	chr11:18713000-18713200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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

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