Variant report

Variant	rs6910841
Chromosome Location	chr6:5520850-5520851
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	chr6:5471238..5471818-chr6:5519987..5520960,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs17140654	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.90[TSI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17140735	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2326612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4960097	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58867246	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59260375	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6909032	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6909197	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6923467	1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6925295	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6938581	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73356354	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356356	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356368	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356373	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356375	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356378	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356381	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356382	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356397	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7760403	1.00[JPT][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019428	chr6:5216835-5627839	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS 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
2	nsv538118	chr6:5216835-5627839	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1034607	chr6:5311590-5573514	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv538120	chr6:5311590-5573514	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv916361	chr6:5315853-5695486	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1023027	chr6:5377308-5556749	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv538121	chr6:5377308-5556749	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1017506	chr6:5443538-5551125	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5488600-5521600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr6:5500400-5525000	Weak transcription	Spleen	Spleen
3	chr6:5501000-5550600	Weak transcription	Pancreas	Pancrea
4	chr6:5508000-5547400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:5509000-5521000	Weak transcription	Fetal Thymus	thymus
6	chr6:5509000-5524400	Weak transcription	Primary B cells from cord blood	blood
7	chr6:5509600-5527400	Weak transcription	Lung	lung
8	chr6:5511200-5546400	Weak transcription	Fetal Intestine Small	intestine
9	chr6:5511400-5540200	Weak transcription	Esophagus	oesophagus
10	chr6:5511400-5568200	Weak transcription	Aorta	Aorta
11	chr6:5512600-5524800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:5512600-5525200	Weak transcription	HSMMtube	muscle
13	chr6:5514000-5537400	Weak transcription	Left Ventricle	heart
14	chr6:5516200-5525800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:5516400-5522800	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr6:5516400-5522800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr6:5516600-5523600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr6:5516800-5523600	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr6:5517200-5523000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr6:5517200-5523000	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr6:5517400-5522800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr6:5517400-5523200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr6:5517800-5523400	Enhancers	Primary T cells from cord blood	blood
24	chr6:5518000-5522800	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr6:5518200-5522800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr6:5518600-5550000	Weak transcription	Right Ventricle	heart
27	chr6:5519800-5521000	Enhancers	Fetal Heart	heart
28	chr6:5520000-5521800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr6:5520400-5521400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:5520400-5521400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:5520400-5521800	Enhancers	Dnd41	blood
32	chr6:5520600-5521600	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr6:5520600-5521800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr6:5520600-5522400	Weak transcription	GM12878-XiMat	blood

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