Variant report

Variant	rs7096357
Chromosome Location	chr10:93873548-93873549
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10786028	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10882023	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10882025	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11186815	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11186817	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11186818	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11186822	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11186829	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11186830	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11186834	0.82[ASN][1000 genomes]
rs11186835	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11186836	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11186838	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11186839	0.82[EUR][1000 genomes]
rs11186841	0.82[EUR][1000 genomes]
rs11186843	0.82[EUR][1000 genomes]
rs12357187	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12571139	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1539468	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1557178	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1571176	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1878424	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1935865	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2096227	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2105364	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2185834	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2421831	0.82[EUR][1000 genomes]
rs2421874	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34658839	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3781230	0.82[EUR][1000 genomes]
rs3781231	0.82[EUR][1000 genomes]
rs3781233	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4933712	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4933717	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56345827	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56705680	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61875208	0.80[EUR][1000 genomes]
rs6583802	0.82[EUR][1000 genomes]
rs66636110	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7067935	0.82[EUR][1000 genomes]
rs7069149	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7071524	0.82[EUR][1000 genomes]
rs7079499	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7084059	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7085684	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7086446	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs766398	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs766399	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9794362	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051226	chr10:93711296-93915586	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv540745	chr10:93711296-93915586	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv895893	chr10:93747260-93875264	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv975763	chr10:93822289-94105956	Enhancers Bivalent Enhancer Strong transcription Active TSS Weak transcription Flanking 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	15 gene(s)	inside rSNPs	diseases
5	nsv1046258	chr10:93866969-94466106	Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93841200-93881600	Weak transcription	Esophagus	oesophagus
2	chr10:93859200-93901400	Weak transcription	Primary B cells from cord blood	blood
3	chr10:93859400-93874800	Weak transcription	Fetal Intestine Large	intestine
4	chr10:93861000-93873600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr10:93861400-93879000	Weak transcription	Adipose Nuclei	Adipose
6	chr10:93862000-93874200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr10:93862000-93881400	Weak transcription	Colon Smooth Muscle	Colon
8	chr10:93862000-93881400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr10:93862000-93883200	Weak transcription	Fetal Stomach	stomach
10	chr10:93863000-93878600	Weak transcription	Gastric	stomach
11	chr10:93863800-93879200	Weak transcription	GM12878-XiMat	blood
12	chr10:93863800-93881400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr10:93863800-93881600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr10:93867400-93876200	Weak transcription	Brain Germinal Matrix	brain
15	chr10:93867400-93881800	Weak transcription	Stomach Mucosa	stomach
16	chr10:93868000-93901800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr10:93868400-93874200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr10:93870200-93875000	Enhancers	HepG2	liver
19	chr10:93870200-93878400	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr10:93870400-93876400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr10:93870800-93881400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr10:93871000-93881600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr10:93871000-93881800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr10:93871000-93882400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr10:93871000-93882400	Weak transcription	Primary T cells from cord blood	blood
26	chr10:93871000-93887200	Weak transcription	Primary B cells from peripheral blood	blood
27	chr10:93871400-93874000	Enhancers	Liver	Liver
28	chr10:93871400-93874000	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr10:93871400-93879000	Weak transcription	Brain Substantia Nigra	brain
30	chr10:93871400-93881400	Weak transcription	Brain Anterior Caudate	brain
31	chr10:93871600-93882000	Weak transcription	Brain Hippocampus Middle	brain
32	chr10:93871800-93881400	Weak transcription	Aorta	Aorta
33	chr10:93871800-93881600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr10:93871800-93884400	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr10:93872200-93873600	Enhancers	Lung	lung
36	chr10:93872400-93873600	Enhancers	Ovary	ovary
37	chr10:93872400-93881400	Weak transcription	Left Ventricle	heart
38	chr10:93872600-93873600	Enhancers	Brain Cingulate Gyrus	brain
39	chr10:93872600-93874200	Enhancers	Fetal Heart	heart
40	chr10:93872800-93874000	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr10:93873000-93878400	Weak transcription	Psoas Muscle	Psoas
42	chr10:93873000-93881400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr10:93873200-93877400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr10:93873400-93873600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr10:93873400-93873600	Enhancers	Pancreas	Pancrea
46	chr10:93873400-93873600	Enhancers	Right Atrium	heart
47	chr10:93873400-93874000	Enhancers	Right Ventricle	heart
48	chr10:93873400-93874000	Enhancers	Small Intestine	intestine
49	chr10:93873400-93874400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr10:93873400-93874400	Enhancers	Fetal Lung	lung

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