Variant report

Variant	rs3779241
Chromosome Location	chr7:33430008-33430009
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10251272	0.81[CHB][hapmap]
rs10253342	0.81[CHB][hapmap]
rs10254276	1.00[CEU][hapmap]
rs10258040	0.89[ASN][1000 genomes]
rs10268593	0.81[CHB][hapmap]
rs10280367	1.00[CEU][hapmap];0.81[CHB][hapmap];0.80[EUR][1000 genomes]
rs12666246	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12666395	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12668181	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12668971	0.84[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs12670765	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12673354	0.81[CHB][hapmap]
rs12674317	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1419920	0.82[ASN][1000 genomes]
rs1419926	0.81[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17395534	1.00[CEU][hapmap]
rs17395966	1.00[CEU][hapmap]
rs17475728	0.81[CHB][hapmap]
rs17476738	0.81[CHB][hapmap]
rs17725162	0.92[ASN][1000 genomes]
rs2041418	0.82[ASN][1000 genomes]
rs2159585	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs35173250	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4341064	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4442031	1.00[CEU][hapmap]
rs57736066	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59066744	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60902947	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6462470	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.83[TSI][hapmap];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6462478	0.92[ASN][1000 genomes]
rs6952538	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6960094	0.81[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6962002	1.00[CEU][hapmap];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6970919	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6973093	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6979138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7777122	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7777332	1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7806498	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.83[TSI][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606610	chr7:33218763-33486316	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1016416	chr7:33241443-33559477	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv916660	chr7:33272493-33506384	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv830944	chr7:33389892-33549882	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33389000-33437400	Weak transcription	Liver	Liver
2	chr7:33403400-33437800	Weak transcription	Brain Substantia Nigra	brain
3	chr7:33403800-33430400	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:33404000-33433000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr7:33408200-33431000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr7:33408200-33434600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr7:33408600-33434400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:33411800-33431000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:33412200-33433200	Weak transcription	Psoas Muscle	Psoas
10	chr7:33417200-33430400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr7:33418000-33438600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr7:33418200-33436400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr7:33418600-33434800	Weak transcription	Fetal Kidney	kidney
14	chr7:33419000-33436800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr7:33420000-33433200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr7:33420000-33435000	Weak transcription	Brain Anterior Caudate	brain
17	chr7:33420400-33431800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:33420400-33435000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr7:33420400-33436400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr7:33420400-33444600	Weak transcription	Left Ventricle	heart
21	chr7:33420600-33431800	Weak transcription	Aorta	Aorta
22	chr7:33420600-33433200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr7:33420600-33435000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:33420600-33435200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr7:33420600-33437800	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr7:33420600-33449200	Weak transcription	Ovary	ovary
27	chr7:33420800-33430200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr7:33420800-33432800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:33420800-33434600	Weak transcription	Fetal Muscle Leg	muscle
30	chr7:33420800-33435000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr7:33420800-33435000	Weak transcription	Fetal Lung	lung
32	chr7:33420800-33437400	Weak transcription	Fetal Intestine Large	intestine
33	chr7:33420800-33437800	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr7:33421000-33439800	Weak transcription	Fetal Stomach	stomach
35	chr7:33421000-33442600	Weak transcription	Pancreas	Pancrea
36	chr7:33422200-33452200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:33422600-33437800	Weak transcription	Brain Angular Gyrus	brain
38	chr7:33424200-33435000	Weak transcription	Primary T cells from cord blood	blood
39	chr7:33424800-33434800	Weak transcription	Primary B cells from peripheral blood	blood
40	chr7:33425200-33435000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr7:33428200-33435200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:33428200-33436200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr7:33428200-33438200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:33428200-33458000	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr7:33428600-33435000	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr7:33429600-33431800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr7:33429800-33433600	Weak transcription	Adipose Nuclei	Adipose

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