Variant report

Variant	rs17140735
Chromosome Location	chr6:5516774-5516775
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	chr6:5511127..5514739-chr6:5516626..5520619,5	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	0.85[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2326612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4960097	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58867246	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59260375	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6909032	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6909197	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6910841	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]
rs6923467	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6925295	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6938581	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73356354	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356356	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356365	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356367	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356368	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356373	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356375	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356376	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356378	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356381	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356382	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73356397	0.90[AMR][1000 genomes];0.95[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:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5466400-5518200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr6:5488600-5521600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr6:5500400-5525000	Weak transcription	Spleen	Spleen
4	chr6:5501000-5550600	Weak transcription	Pancreas	Pancrea
5	chr6:5508000-5547400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:5508200-5516800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr6:5508200-5519400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr6:5508600-5517200	Weak transcription	Primary T cells from cord blood	blood
9	chr6:5509000-5517200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr6:5509000-5519400	Weak transcription	Primary B cells from peripheral blood	blood
11	chr6:5509000-5521000	Weak transcription	Fetal Thymus	thymus
12	chr6:5509000-5524400	Weak transcription	Primary B cells from cord blood	blood
13	chr6:5509600-5527400	Weak transcription	Lung	lung
14	chr6:5510600-5518200	Weak transcription	Fetal Heart	heart
15	chr6:5511200-5546400	Weak transcription	Fetal Intestine Small	intestine
16	chr6:5511400-5518200	Weak transcription	Gastric	stomach
17	chr6:5511400-5518200	Weak transcription	Right Ventricle	heart
18	chr6:5511400-5540200	Weak transcription	Esophagus	oesophagus
19	chr6:5511400-5568200	Weak transcription	Aorta	Aorta
20	chr6:5512000-5517200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr6:5512400-5517200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:5512600-5524800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:5512600-5525200	Weak transcription	HSMMtube	muscle
24	chr6:5513000-5519200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:5514000-5518200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:5514000-5537400	Weak transcription	Left Ventricle	heart
27	chr6:5514200-5518200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:5515000-5518800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr6:5516200-5525800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr6:5516400-5522800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr6:5516400-5522800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr6:5516600-5520600	Enhancers	GM12878-XiMat	blood
33	chr6:5516600-5523600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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