Variant report

Variant	rs6734446
Chromosome Location	chr2:179249019-179249020
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10497515	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs10497516	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12612917	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12613303	1.00[CEU][hapmap]
rs12615980	0.83[EUR][1000 genomes]
rs12616943	0.89[EUR][1000 genomes]
rs12619401	0.83[EUR][1000 genomes]
rs16866323	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2195070	1.00[CEU][hapmap]
rs2276619	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2276620	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3731756	0.83[EUR][1000 genomes]
rs3731758	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs3765020	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs3816073	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs4491754	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55714261	0.89[EUR][1000 genomes]
rs55831332	0.99[ASN][1000 genomes]
rs56065555	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56233214	0.94[EUR][1000 genomes]
rs56357262	0.89[EUR][1000 genomes]
rs62176089	0.81[ASN][1000 genomes]
rs6736173	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6736304	1.00[EUR][1000 genomes]
rs6757474	1.00[CEU][hapmap]
rs6757481	1.00[CEU][hapmap]
rs73034339	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73034346	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73034359	1.00[EUR][1000 genomes]
rs73034362	1.00[EUR][1000 genomes]
rs73034364	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73034377	0.89[EUR][1000 genomes]
rs7584420	0.94[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834466	chr2:179140792-179284778	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179201800-179253600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr2:179201800-179268200	Weak transcription	HSMM	muscle
3	chr2:179209200-179253000	Weak transcription	Esophagus	oesophagus
4	chr2:179210800-179257200	Weak transcription	Pancreas	Pancrea
5	chr2:179225000-179257800	Weak transcription	Lung	lung
6	chr2:179226600-179257200	Weak transcription	Gastric	stomach
7	chr2:179232000-179254200	Weak transcription	Hela-S3	cervix
8	chr2:179235600-179251600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr2:179237400-179252200	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr2:179238400-179251400	Weak transcription	Fetal Intestine Large	intestine
11	chr2:179240000-179258200	Weak transcription	NHEK	skin
12	chr2:179240200-179256800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:179240800-179249200	Weak transcription	Aorta	Aorta
14	chr2:179240800-179252000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr2:179240800-179253800	Weak transcription	Right Ventricle	heart
16	chr2:179241800-179262600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr2:179242200-179254600	Weak transcription	Ovary	ovary
18	chr2:179242200-179258600	Weak transcription	Brain Germinal Matrix	brain
19	chr2:179242400-179253000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:179242600-179250000	Weak transcription	Fetal Stomach	stomach
21	chr2:179245800-179251400	Strong transcription	Skeletal Muscle Female	skeletal muscle
22	chr2:179246000-179256200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr2:179246200-179250400	Weak transcription	K562	blood
24	chr2:179246400-179251400	Weak transcription	HUVEC	blood vessel
25	chr2:179246600-179257200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr2:179246800-179250000	Weak transcription	Osteobl	bone
27	chr2:179247000-179254600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:179247200-179249200	Strong transcription	HMEC	breast
29	chr2:179247200-179253600	Strong transcription	Liver	Liver
30	chr2:179247600-179249200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:179247600-179249600	Strong transcription	Brain Anterior Caudate	brain
32	chr2:179247600-179249800	Strong transcription	Fetal Brain Female	brain
33	chr2:179247800-179249400	Strong transcription	Cortex derived primary cultured neurospheres	brain
34	chr2:179247800-179249600	Strong transcription	Brain Angular Gyrus	brain
35	chr2:179247800-179249600	Strong transcription	Psoas Muscle	Psoas
36	chr2:179247800-179249800	Strong transcription	Fetal Muscle Trunk	muscle
37	chr2:179247800-179250800	Strong transcription	HSMMtube	muscle
38	chr2:179247800-179254600	Strong transcription	Brain Inferior Temporal Lobe	brain
39	chr2:179248000-179249400	Strong transcription	Left Ventricle	heart
40	chr2:179248000-179251000	Strong transcription	NH-A	brain
41	chr2:179248000-179255000	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr2:179248200-179249200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr2:179248200-179249400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr2:179248200-179249400	Strong transcription	Fetal Brain Male	brain
45	chr2:179248200-179257200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr2:179248600-179254400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:179248800-179249200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:179248800-179249600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:179248800-179249600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr2:179249000-179251800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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