Variant report

Variant	rs10793245
Chromosome Location	chr11:76946324-76946325
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:76940055..76942991-chr11:76943118..76946420,3	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10793244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10793246	0.94[JPT][hapmap]
rs10899364	0.94[JPT][hapmap]
rs10899365	0.94[JPT][hapmap]
rs10899369	0.94[JPT][hapmap]
rs11237145	0.95[JPT][hapmap]
rs11237146	0.94[JPT][hapmap]
rs11237147	0.94[JPT][hapmap]
rs11607378	0.81[EUR][1000 genomes]
rs12274255	0.95[JPT][hapmap]
rs12287216	0.95[JPT][hapmap]
rs12287680	0.95[JPT][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes]
rs1613357	0.95[JPT][hapmap]
rs1618188	0.94[JPT][hapmap]
rs1620915	0.95[JPT][hapmap]
rs1670451	0.94[JPT][hapmap]
rs1670452	0.95[JPT][hapmap]
rs1670453	0.95[JPT][hapmap]
rs1670460	0.89[JPT][hapmap]
rs1793466	0.89[JPT][hapmap]
rs1793467	0.89[JPT][hapmap]
rs1793488	0.94[JPT][hapmap]
rs1894214	0.94[JPT][hapmap]
rs1901821	0.96[CEU][hapmap];0.93[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1946005	0.94[JPT][hapmap]
rs2007466	0.80[EUR][1000 genomes]
rs2602486	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28420990	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2853096	0.89[JPT][hapmap]
rs4433591	0.80[EUR][1000 genomes]
rs4944153	0.86[EUR][1000 genomes]
rs4944155	0.81[EUR][1000 genomes]
rs4945162	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs4945166	0.87[CEU][hapmap];0.81[EUR][1000 genomes]
rs4945168	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57129983	0.81[EUR][1000 genomes]
rs61901769	0.81[EUR][1000 genomes]
rs7104166	0.94[JPT][hapmap]
rs7104295	0.95[JPT][hapmap]
rs7118869	0.83[CEU][hapmap]
rs7121483	0.95[JPT][hapmap]
rs7123198	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7928731	0.81[EUR][1000 genomes]
rs7938075	0.95[JPT][hapmap]
rs948971	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9634031	0.88[JPT][hapmap]

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	nsv534515	chr11:76900813-77035769	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1048360	chr11:76900813-77387933	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv541089	chr11:76900813-77387933	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1049603	chr11:76900813-77520411	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv541090	chr11:76900813-77520411	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76937400-76948000	Weak transcription	Fetal Intestine Large	intestine
2	chr11:76942800-76947600	Weak transcription	Liver	Liver
3	chr11:76944600-76954600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:76945000-76947600	Weak transcription	Stomach Mucosa	stomach

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