Variant report

Variant	rs6451341
Chromosome Location	chr5:37743077-37743078
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10071815	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10076102	1.00[CHD][hapmap]
rs13188890	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1549251	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1549252	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs16903703	0.84[LWK][hapmap]
rs16903704	0.80[LWK][hapmap]
rs28377651	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28874633	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2910798	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2972941	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2973074	0.97[EUR][1000 genomes]
rs2973085	1.00[CEU][hapmap]
rs41270339	0.86[EUR][1000 genomes]
rs55654436	0.86[EUR][1000 genomes]
rs56279820	0.86[EUR][1000 genomes]
rs59898254	1.00[EUR][1000 genomes]
rs67885658	0.86[EUR][1000 genomes]
rs72743159	0.86[EUR][1000 genomes]
rs72743164	0.86[EUR][1000 genomes]
rs72743166	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72743167	0.86[EUR][1000 genomes]
rs72743169	0.86[EUR][1000 genomes]
rs72743170	0.86[EUR][1000 genomes]
rs72743176	0.86[EUR][1000 genomes]
rs72743180	0.86[EUR][1000 genomes]
rs72743185	0.86[EUR][1000 genomes]
rs72743187	0.86[EUR][1000 genomes]
rs72743190	0.86[EUR][1000 genomes]
rs72743192	0.86[EUR][1000 genomes]
rs72743193	0.86[EUR][1000 genomes]
rs72743196	0.86[EUR][1000 genomes]
rs72743200	0.86[EUR][1000 genomes]
rs72743201	0.86[EUR][1000 genomes]
rs72743202	0.86[EUR][1000 genomes]
rs72745106	0.86[EUR][1000 genomes]
rs72745108	0.86[EUR][1000 genomes]
rs7448783	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7705963	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7722257	1.00[CEU][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7737640	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9283746	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949716	chr5:37179341-37967352	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
2	nsv1023871	chr5:37330018-37804744	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv537729	chr5:37330018-37804744	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv432744	chr5:37374124-37743077	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv597846	chr5:37430215-37813591	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv881383	chr5:37485316-37773877	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37685200-37743200	Weak transcription	Gastric	stomach
2	chr5:37697000-37743800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr5:37717800-37756200	Weak transcription	Right Ventricle	heart
4	chr5:37718400-37743200	Weak transcription	Aorta	Aorta
5	chr5:37718400-37745400	Weak transcription	Pancreas	Pancrea
6	chr5:37718400-37755800	Weak transcription	Spleen	Spleen
7	chr5:37721400-37764200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr5:37722400-37743200	Weak transcription	Esophagus	oesophagus
9	chr5:37727600-37745400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr5:37728000-37757200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr5:37728000-37758800	Weak transcription	Brain Germinal Matrix	brain
12	chr5:37728400-37743200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:37728400-37745400	Weak transcription	Thymus	Thymus
14	chr5:37728800-37754400	Weak transcription	Placenta	Placenta
15	chr5:37729000-37746000	Weak transcription	Fetal Thymus	thymus
16	chr5:37729400-37753200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr5:37729600-37743200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr5:37729600-37745000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:37729600-37755800	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr5:37730000-37749800	Weak transcription	HepG2	liver
21	chr5:37730200-37752000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr5:37730200-37757000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr5:37730400-37752200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr5:37731400-37743200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr5:37731400-37745400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr5:37731600-37745600	Weak transcription	Fetal Lung	lung
27	chr5:37735800-37744600	Strong transcription	Primary B cells from peripheral blood	blood
28	chr5:37736000-37743200	Weak transcription	Lung	lung
29	chr5:37736200-37752200	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr5:37736200-37752400	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr5:37736400-37744000	Weak transcription	Fetal Brain Male	brain
32	chr5:37737400-37744600	Strong transcription	Primary T cells from cord blood	blood
33	chr5:37737800-37754000	Weak transcription	Left Ventricle	heart
34	chr5:37738400-37744400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr5:37738400-37757200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr5:37738600-37745200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr5:37738800-37756400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr5:37738800-37757400	Weak transcription	Brain Anterior Caudate	brain
39	chr5:37739000-37743200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:37739000-37743400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr5:37739000-37757200	Weak transcription	Duodenum Mucosa	Duodenum
42	chr5:37739200-37751200	Weak transcription	NHEK	skin
43	chr5:37739200-37757600	Weak transcription	A549	lung
44	chr5:37739400-37751200	Weak transcription	HMEC	breast
45	chr5:37739400-37752800	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr5:37739600-37747400	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr5:37739600-37748400	Weak transcription	Brain Hippocampus Middle	brain
48	chr5:37739600-37757200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:37740200-37743400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:37740800-37743800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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