Variant report

Variant	rs2793253
Chromosome Location	chr6:5039243-5039244
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs12194104	0.81[ASN][1000 genomes]
rs12200195	0.88[ASN][1000 genomes]
rs1627212	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1749155	0.93[EUR][1000 genomes]
rs1771868	0.93[EUR][1000 genomes]
rs1771873	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771874	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1815673	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1815674	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1815675	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2002380	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2147705	0.93[EUR][1000 genomes]
rs2764128	0.93[EUR][1000 genomes]
rs2764131	0.93[EUR][1000 genomes]
rs2764133	0.93[EUR][1000 genomes]
rs2764140	0.93[EUR][1000 genomes]
rs2764144	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2764147	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2764150	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2764153	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764154	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764170	0.93[EUR][1000 genomes]
rs2764189	0.93[EUR][1000 genomes]
rs2793239	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2793246	0.91[EUR][1000 genomes]
rs2793252	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2793254	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793256	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793257	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793258	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2793259	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2985677	0.93[EUR][1000 genomes]
rs2994695	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2994696	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4246072	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4281005	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57919800	0.82[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs59552394	0.81[ASN][1000 genomes]
rs62385159	0.88[ASN][1000 genomes]
rs62386470	0.88[ASN][1000 genomes]
rs62386471	0.81[ASN][1000 genomes]
rs726743	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs754334	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs811259	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs877229	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9378925	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv2422499	chr6:4745428-5073222	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv830577	chr6:4834567-5050544	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv462622	chr6:4904380-5172009	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv600871	chr6:4904380-5172009	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1033905	chr6:4955826-5080904	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv600872	chr6:4975313-5342190	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
8	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
9	nsv1017380	chr6:5007870-5152551	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
10	esv3381089	chr6:5036503-5040201	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
11	esv3472034	chr6:5036834-5039527	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	n/a
12	esv2548026	chr6:5036847-5039982	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
13	esv6488	chr6:5036993-5039414	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
14	esv1991955	chr6:5037086-5039355	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
15	esv3472035	chr6:5037116-5039274	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
16	esv3357513	chr6:5037139-5039277	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
17	esv3327309	chr6:5037142-5039303	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
18	esv1001530	chr6:5037151-5039257	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
19	esv3396813	chr6:5037161-5039258	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
20	esv3472033	chr6:5037172-5039256	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
21	esv3472032	chr6:5037179-5039253	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
22	nsv513295	chr6:5037182-5039260	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
23	esv3833	chr6:5037213-5039289	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5027200-5047200	Weak transcription	Adipose Nuclei	Adipose
2	chr6:5031200-5042800	Weak transcription	Ovary	ovary
3	chr6:5031600-5042800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr6:5031800-5043800	Weak transcription	Spleen	Spleen
5	chr6:5033400-5046000	Weak transcription	Fetal Intestine Small	intestine
6	chr6:5033400-5048600	Weak transcription	Aorta	Aorta
7	chr6:5034400-5045200	Weak transcription	Fetal Stomach	stomach
8	chr6:5034800-5045600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr6:5034800-5047400	Weak transcription	Esophagus	oesophagus
10	chr6:5035000-5047400	Weak transcription	Primary B cells from cord blood	blood
11	chr6:5035400-5047800	Weak transcription	Primary B cells from peripheral blood	blood
12	chr6:5035800-5042600	Weak transcription	Placenta	Placenta
13	chr6:5036600-5044800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr6:5037000-5050800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:5037200-5041000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:5037200-5044800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr6:5037200-5045200	Weak transcription	Fetal Muscle Leg	muscle
18	chr6:5037200-5046000	Weak transcription	Fetal Muscle Trunk	muscle

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