Variant report

Variant	rs7071536
Chromosome Location	chr10:5903518-5903519
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:5853453..5856522-chr10:5901378..5904221,3	K562	blood:
2	chr10:5903402..5905306-chr10:5930976..5933543,3	MCF-7	breast:
3	chr10:5853575..5857221-chr10:5900529..5905112,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000134461	Chromatin interaction
ENSG00000057608	Chromatin interaction
ENSG00000134452	Chromatin interaction
ENSG00000272764	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1052420	0.84[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]
rs1707228	0.82[CHB][hapmap];0.95[CHD][hapmap];0.92[JPT][hapmap]
rs2253422	0.84[JPT][hapmap]
rs2274030	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs2669123	0.89[ASN][1000 genomes]
rs2669124	0.84[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap]
rs2985042	0.84[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]
rs2985043	0.84[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]
rs2985044	0.84[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]
rs593026	1.00[CHD][hapmap];0.82[JPT][hapmap]
rs596156	0.84[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap]
rs599394	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs608197	0.84[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]
rs609269	0.84[CHB][hapmap];0.95[CHD][hapmap];0.84[JPT][hapmap]
rs615879	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs617165	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs61832916	1.00[ASN][1000 genomes]
rs622252	0.84[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]
rs626040	0.84[CHB][hapmap];0.95[CHD][hapmap];0.92[JPT][hapmap]
rs628844	0.92[JPT][hapmap]
rs646406	0.84[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap]
rs646490	0.84[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap]
rs647391	0.84[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap]
rs661411	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs662701	0.84[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]
rs664577	0.84[CHB][hapmap];0.95[CHD][hapmap];0.84[JPT][hapmap]
rs666831	0.83[CHB][hapmap];0.84[JPT][hapmap]
rs673496	0.84[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap]
rs675416	0.84[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap]
rs679610	0.84[CHB][hapmap]
rs684557	0.81[CHB][hapmap]
rs7084904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7091817	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7098957	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73614644	0.92[ASN][1000 genomes]
rs792347	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs811561	0.84[CHB][hapmap];0.92[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv831775	chr10:5804335-6000849	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv5654	chr10:5868365-5930634	Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv825229	chr10:5886905-5967697	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv466722	chr10:5893268-5916201	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv549904	chr10:5893268-5916201	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv437655	chr10:5900973-5910361	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv520941	chr10:5903518-5904918	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5888800-5904400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:5894600-5908600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:5894600-5908600	Weak transcription	K562	blood
4	chr10:5894600-5916800	Weak transcription	Spleen	Spleen
5	chr10:5896200-5912200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr10:5896400-5918200	Weak transcription	Fetal Lung	lung
7	chr10:5896600-5903800	Weak transcription	Fetal Stomach	stomach
8	chr10:5897000-5903800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr10:5899000-5904200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr10:5899800-5904200	Weak transcription	Ovary	ovary
11	chr10:5899800-5905000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr10:5900000-5904000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:5900000-5916600	Weak transcription	Pancreas	Pancrea
14	chr10:5900400-5916200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr10:5900600-5916200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr10:5900800-5910600	Weak transcription	Brain Germinal Matrix	brain
17	chr10:5901000-5904200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:5901000-5916600	Weak transcription	Gastric	stomach
19	chr10:5901200-5904200	Weak transcription	Brain Angular Gyrus	brain
20	chr10:5901200-5918200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:5901400-5905000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr10:5901400-5915200	Weak transcription	Brain Hippocampus Middle	brain
23	chr10:5901600-5904200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr10:5901600-5912600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr10:5901600-5915600	Weak transcription	Brain Anterior Caudate	brain
26	chr10:5901800-5904200	Weak transcription	Fetal Intestine Small	intestine
27	chr10:5901800-5910800	Weak transcription	Fetal Brain Female	brain
28	chr10:5902000-5904000	Enhancers	GM12878-XiMat	blood
29	chr10:5902000-5904800	Enhancers	Placenta	Placenta
30	chr10:5902200-5904600	Enhancers	NHDF-Ad	bronchial
31	chr10:5902200-5905000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr10:5902200-5912600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr10:5902400-5904400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr10:5902400-5905000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr10:5902400-5908600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:5902400-5918200	Weak transcription	Primary T cells from cord blood	blood
37	chr10:5902600-5904600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr10:5902600-5910200	Weak transcription	Fetal Muscle Leg	muscle
39	chr10:5902800-5903600	Weak transcription	NHLF	lung
40	chr10:5902800-5916200	Weak transcription	Fetal Intestine Large	intestine
41	chr10:5902800-5916600	Weak transcription	Brain Substantia Nigra	brain
42	chr10:5902800-5918000	Weak transcription	Lung	lung
43	chr10:5903000-5903800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:5903000-5903800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr10:5903000-5904400	Enhancers	HSMM	muscle
46	chr10:5903000-5904600	Enhancers	Muscle Satellite Cultured Cells	--
47	chr10:5903000-5905200	Enhancers	HepG2	liver
48	chr10:5903000-5912400	Weak transcription	Fetal Heart	heart
49	chr10:5903000-5915400	Weak transcription	Duodenum Mucosa	Duodenum
50	chr10:5903200-5903600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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