Variant report

Variant	rs9496351
Chromosome Location	chr6:142676495-142676496
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:142667887..142670246-chr6:142675631..142677996,2	MCF-7	breast:
2	chr6:142675895..142678114-chr6:142681303..142684417,3	MCF-7	breast:
3	chr6:142673899..142675482-chr6:142676247..142678997,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs13437156	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1411147	1.00[AMR][1000 genomes]
rs6921559	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484627	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484628	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484629	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484634	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484635	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484636	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484638	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484640	1.00[AMR][1000 genomes]
rs9484641	1.00[AMR][1000 genomes]
rs9484644	1.00[AMR][1000 genomes]
rs9496336	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496350	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496359	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496362	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496363	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496375	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496376	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496381	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496383	1.00[AMR][1000 genomes]
rs9496384	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496385	1.00[AMR][1000 genomes]
rs9496386	1.00[AMR][1000 genomes]
rs9496387	1.00[AMR][1000 genomes]
rs9496393	1.00[AMR][1000 genomes]
rs9496407	1.00[AMR][1000 genomes]
rs9496408	1.00[AMR][1000 genomes]
rs9496410	1.00[AMR][1000 genomes]

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	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830825	chr6:142585242-142752575	Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142654800-142676600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:142657400-142678800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:142665600-142680200	Weak transcription	HUVEC	blood vessel
4	chr6:142666000-142677000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:142670800-142676600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:142670800-142676600	Weak transcription	Thymus	Thymus
7	chr6:142671400-142679400	Weak transcription	Liver	Liver
8	chr6:142672600-142676600	Strong transcription	HepG2	liver
9	chr6:142672600-142680800	Weak transcription	Fetal Brain Male	brain
10	chr6:142674400-142678000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:142674600-142676600	Enhancers	A549	lung
12	chr6:142674800-142676600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:142674800-142680400	Enhancers	Fetal Lung	lung
14	chr6:142675800-142678000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr6:142675800-142679200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr6:142676200-142676600	Enhancers	Primary T cells from cord blood	blood
17	chr6:142676200-142676600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:142676400-142676600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:142676400-142676800	Enhancers	Primary hematopoietic stem cells	blood
20	chr6:142676400-142677000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:142676400-142677600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:142676400-142681000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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