Variant report

Variant	rs34841357
Chromosome Location	chr7:5049923-5049924
allele	A/C
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:19)

rs_ID	r²[population]
rs12668616	0.87[EUR][1000 genomes]
rs12670920	0.88[AMR][1000 genomes]
rs12674330	0.87[EUR][1000 genomes]
rs13233801	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13234950	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13235865	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28394032	0.89[ASN][1000 genomes]
rs34404989	0.86[EUR][1000 genomes]
rs34544476	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34823543	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35801949	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36026500	0.88[EUR][1000 genomes]
rs36046535	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4073330	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4613891	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62444279	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62444280	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62444314	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9690559	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529538	chr7:4509189-5151503	Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv530968	chr7:4572250-5418004	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv1031697	chr7:4677463-5241790	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv538704	chr7:4677463-5241790	Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	nsv8033	chr7:4802287-5086597	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv1022678	chr7:4810626-5113387	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv538705	chr7:4810626-5113387	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv1021170	chr7:4831361-5058033	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv538706	chr7:4831361-5058033	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv1033855	chr7:4862677-5069764	Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
12	nsv1019120	chr7:4929653-5138409	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
13	nsv917078	chr7:4962123-5151633	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
14	nsv525289	chr7:5003373-5083741	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
15	nsv966749	chr7:5036761-5098568	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5029800-5051200	Weak transcription	Psoas Muscle	Psoas
2	chr7:5029800-5059400	Weak transcription	NHDF-Ad	bronchial
3	chr7:5036000-5051000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr7:5036600-5064200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr7:5037000-5051600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr7:5037000-5054400	Weak transcription	Small Intestine	intestine
7	chr7:5037000-5058600	Weak transcription	Colon Smooth Muscle	Colon
8	chr7:5037200-5050600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:5037200-5050800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr7:5037200-5059400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr7:5037600-5050600	Weak transcription	Aorta	Aorta
12	chr7:5037600-5062000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr7:5037600-5064800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr7:5037800-5050400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr7:5038000-5051800	Weak transcription	K562	blood
16	chr7:5038000-5061400	Weak transcription	HSMMtube	muscle
17	chr7:5038200-5051000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr7:5038200-5066000	Weak transcription	Brain Substantia Nigra	brain
19	chr7:5038800-5051200	Weak transcription	Osteobl	bone
20	chr7:5038800-5067600	Weak transcription	Gastric	stomach
21	chr7:5038800-5085000	Weak transcription	Spleen	Spleen
22	chr7:5039000-5051200	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr7:5039000-5052000	Weak transcription	NHLF	lung
24	chr7:5039000-5058600	Weak transcription	Brain Angular Gyrus	brain
25	chr7:5039000-5076200	Weak transcription	Brain Anterior Caudate	brain
26	chr7:5039000-5078400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr7:5039200-5060400	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr7:5039400-5059200	Weak transcription	Thymus	Thymus
29	chr7:5039400-5085000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr7:5040000-5054000	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr7:5040200-5059600	Weak transcription	Adipose Nuclei	Adipose
32	chr7:5041800-5066200	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr7:5043000-5058600	Weak transcription	Stomach Smooth Muscle	stomach
34	chr7:5045000-5063400	Weak transcription	Pancreas	Pancrea
35	chr7:5045400-5050200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:5045400-5065200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:5045600-5050600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr7:5045800-5050200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr7:5045800-5050200	Weak transcription	NH-A	brain
40	chr7:5045800-5050600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:5045800-5059000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr7:5045800-5059400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr7:5045800-5059800	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr7:5046800-5051400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:5046800-5051800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:5047400-5050000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr7:5047600-5063600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr7:5047800-5051400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr7:5048000-5050800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr7:5048000-5051000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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