Variant report

Variant	rs802755
Chromosome Location	chr6:128254688-128254689
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1089649	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1089651	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs156062	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs156063	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs156064	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs166581	0.90[EUR][1000 genomes]
rs198523	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs198524	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes]
rs270022	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs404528	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs413612	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs428016	0.96[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs699416	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs699417	0.96[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs699418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs699419	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs699420	1.00[ASN][1000 genomes]
rs802704	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs802708	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs802709	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs802712	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs802713	0.97[EUR][1000 genomes]
rs802715	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs802716	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs802752	0.92[EUR][1000 genomes]
rs802753	0.88[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs802756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][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	esv1849854	chr6:128143774-128287313	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv1024516	chr6:128184182-128298278	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128246000-128260200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:128253600-128255400	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr6:128253600-128255800	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr6:128253800-128254800	Enhancers	Primary T cells fromperipheralblood	blood
5	chr6:128253800-128255400	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr6:128253800-128255400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr6:128253800-128255600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr6:128254200-128255400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:128254200-128255400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr6:128254200-128271400	Weak transcription	Thymus	Thymus
11	chr6:128254400-128255400	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr6:128254400-128255400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr6:128254400-128255600	Enhancers	Primary T cells from cord blood	blood
14	chr6:128254400-128256600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr6:128254400-128260200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr6:128254600-128255600	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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