Variant report

Variant	rs10208436
Chromosome Location	chr2:86936496-86936497
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:86850404..86852440-chr2:86934384..86936918,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000239305	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10175293	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10177148	0.90[JPT][hapmap];1.00[AFR][1000 genomes]
rs10197244	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10201581	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10207306	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs10207541	0.91[JPT][hapmap];1.00[AFR][1000 genomes]
rs12467185	1.00[AFR][1000 genomes]
rs12476889	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs12477946	0.90[JPT][hapmap]
rs13410422	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13411177	0.90[ASN][1000 genomes]
rs13412314	1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs13413566	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13416756	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs13430105	1.00[AFR][1000 genomes]
rs13431959	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2367368	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28528854	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28662199	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28851847	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28889570	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4402760	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6716259	1.00[CHB][hapmap]
rs6735599	0.90[ASN][1000 genomes]
rs7349247	0.90[ASN][1000 genomes]
rs7420475	1.00[AFR][1000 genomes]
rs7570057	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7577266	0.90[JPT][hapmap]

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	nsv532724	chr2:86622295-87086407	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv961802	chr2:86933414-86958321	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86933600-86941600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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