Variant report

Variant	rs9341901
Chromosome Location	chr6:82522770-82522771
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:82458586..82464036-chr6:82521971..82527096,10	MCF-7	breast:

Variant related genes	Relation type
ENSG00000112773	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs16893526	0.80[YRI][hapmap]
rs1931626	1.00[CEU][hapmap];0.89[CHB][hapmap];0.80[JPT][hapmap];0.91[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1931627	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1931628	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1931629	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs194612	0.83[CEU][hapmap]
rs4476879	0.82[YRI][hapmap]
rs6925561	1.00[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9344224	1.00[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9344225	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9353030	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9353031	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830712	chr6:82491029-82654531	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82517200-82530600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:82518800-82524200	Weak transcription	NHLF	lung
3	chr6:82519200-82523000	Weak transcription	Adipose Nuclei	Adipose
4	chr6:82519200-82524200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:82519200-82524200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:82519200-82524200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:82519200-82528800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:82519400-82524200	Weak transcription	Osteobl	bone
9	chr6:82521600-82524000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr6:82521800-82523000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:82522000-82522800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
12	chr6:82522000-82522800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr6:82522000-82522800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:82522000-82523400	Enhancers	Primary B cells from peripheral blood	blood
15	chr6:82522400-82523000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:82522400-82523000	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr6:82522400-82523200	Enhancers	HepG2	liver
18	chr6:82522600-82523200	Enhancers	Primary B cells from cord blood	blood
19	chr6:82522600-82523400	Enhancers	Primary hematopoietic stem cells	blood
20	chr6:82522600-82524000	Enhancers	Primary neutrophils fromperipheralblood	blood

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