Variant report

Variant	rs73294820
Chromosome Location	chr10:49560458-49560459
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:49560371..49562620-chr10:49566484..49568463,2	K562	blood:
2	chr10:49551581..49553904-chr10:49558075..49560720,3	K562	blood:
3	chr10:49559917..49561809-chr10:49572353..49575219,2	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs59420160	1.00[AFR][1000 genomes]
rs61020424	1.00[AFR][1000 genomes]
rs61137889	1.00[AFR][1000 genomes]
rs73293150	1.00[AFR][1000 genomes]
rs73293155	1.00[AFR][1000 genomes]
rs73293165	1.00[AFR][1000 genomes]
rs73293173	1.00[AFR][1000 genomes]
rs73293176	1.00[AFR][1000 genomes]
rs73293188	1.00[AFR][1000 genomes]
rs73293525	1.00[AFR][1000 genomes]
rs73293535	1.00[AFR][1000 genomes]
rs73293546	1.00[AFR][1000 genomes]
rs73294804	1.00[AFR][1000 genomes]
rs73296759	1.00[AFR][1000 genomes]
rs73296764	1.00[AFR][1000 genomes]
rs73296795	1.00[AFR][1000 genomes]
rs73296802	1.00[AFR][1000 genomes]
rs73307994	1.00[AFR][1000 genomes]
rs73309908	1.00[AFR][1000 genomes]
rs73309909	1.00[AFR][1000 genomes]
rs73309919	1.00[AFR][1000 genomes]
rs73309924	1.00[AFR][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	nsv895366	chr10:49299274-49576454	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv467190	chr10:49402084-49576878	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv550811	chr10:49402084-49576878	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
5	nsv6587	chr10:49526329-49571804	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	3 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	chr10:49542800-49568000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:49543000-49576200	Weak transcription	Right Atrium	heart
3	chr10:49550400-49560800	Weak transcription	Psoas Muscle	Psoas
4	chr10:49552600-49568800	Weak transcription	NHDF-Ad	bronchial
5	chr10:49559600-49568000	Weak transcription	Ovary	ovary
6	chr10:49559600-49572000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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