Variant report

Variant	rs3776969
Chromosome Location	chr5:80006982-80006983
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:79958590..79961048-chr5:80005503..80007376,2	K562	blood:
2	chr5:80006234..80009005-chr5:80012487..80014948,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1428030	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805355	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];0.91[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap]
rs181747	0.89[ASN][1000 genomes]
rs2195291	0.82[CEU][hapmap]
rs3776970	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3776971	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3797877	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]
rs3797885	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3797886	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3797896	0.81[AMR][1000 genomes]
rs3816729	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4704680	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4704681	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4704683	0.89[AMR][1000 genomes]
rs6151628	0.82[CEU][hapmap]
rs6151639	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.96[LWK][hapmap];1.00[TSI][hapmap]
rs6151685	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6151705	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6151714	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6151769	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6151789	0.84[AMR][1000 genomes]
rs6151826	1.00[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap]
rs6151865	0.81[AMR][1000 genomes]
rs6879843	0.86[AMR][1000 genomes]
rs6881898	0.89[AMR][1000 genomes]
rs6894961	0.83[AMR][1000 genomes]
rs73125417	0.87[AMR][1000 genomes]
rs7711890	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs836812	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024844	chr5:79862428-80860430	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv882231	chr5:79984714-80187929	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv598747	chr5:79996632-80322712	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79951600-80015600	Weak transcription	Small Intestine	intestine
2	chr5:79956400-80015600	Weak transcription	Psoas Muscle	Psoas
3	chr5:79962800-80015600	Weak transcription	A549	lung
4	chr5:79963600-80038600	Weak transcription	Right Ventricle	heart
5	chr5:79964800-80057800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:79965000-80021400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr5:79969600-80010600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr5:79971600-80022200	Weak transcription	HMEC	breast
9	chr5:79971800-80015400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr5:79971800-80112400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr5:79972400-80010400	Weak transcription	NHEK	skin
12	chr5:79972400-80037000	Weak transcription	Brain Cingulate Gyrus	brain
13	chr5:79973200-80021600	Weak transcription	NH-A	brain
14	chr5:79973400-80008800	Weak transcription	Brain Anterior Caudate	brain
15	chr5:79974000-80021200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr5:79975200-80022800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr5:79975600-80015200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr5:79975600-80022000	Weak transcription	Rectal Smooth Muscle	rectum
19	chr5:79975800-80007000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr5:79975800-80008800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:79975800-80009200	Weak transcription	Pancreas	Pancrea
22	chr5:79975800-80015600	Weak transcription	Brain Substantia Nigra	brain
23	chr5:79975800-80015800	Weak transcription	Fetal Brain Female	brain
24	chr5:79976000-80010400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr5:79979200-80013800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:79979800-80009000	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr5:79979800-80015600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:79980000-80015800	Weak transcription	Fetal Kidney	kidney
29	chr5:79983400-80021600	Weak transcription	Brain Angular Gyrus	brain
30	chr5:79985000-80100600	Weak transcription	Brain Germinal Matrix	brain
31	chr5:79992400-80021000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr5:79994400-80016000	Weak transcription	Colon Smooth Muscle	Colon
33	chr5:79995800-80007800	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr5:79997000-80009600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr5:79997400-80009200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr5:79998400-80021400	Weak transcription	K562	blood
37	chr5:79998400-80021600	Weak transcription	Spleen	Spleen
38	chr5:79998600-80008600	Weak transcription	Brain Hippocampus Middle	brain
39	chr5:79998600-80015600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr5:79998600-80051000	Weak transcription	Fetal Brain Male	brain
41	chr5:79998800-80007000	Weak transcription	Aorta	Aorta
42	chr5:79998800-80022200	Weak transcription	Gastric	stomach
43	chr5:79998800-80109400	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr5:79999800-80021200	Weak transcription	Placenta	Placenta
45	chr5:80000000-80007000	Weak transcription	Lung	lung
46	chr5:80000000-80010600	Weak transcription	HSMM	muscle
47	chr5:80000000-80015600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr5:80000000-80021200	Weak transcription	Osteobl	bone
49	chr5:80000200-80007200	Weak transcription	Ovary	ovary
50	chr5:80000200-80010600	Weak transcription	Primary B cells from peripheral blood	blood

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