Variant report

Variant	rs7844431
Chromosome Location	chr8:95795088-95795089
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:95789722..95791429-chr8:95793074..95795753,2	MCF-7	breast:
2	chr8:95794630..95797325-chr8:95807437..95809002,2	K562	blood:

Variant related genes	Relation type
ENSG00000156162	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10090736	0.81[ASN][1000 genomes]
rs10095896	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs10100860	0.80[YRI][hapmap]
rs10101523	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11987988	0.84[ASN][1000 genomes]
rs11995317	0.84[ASN][1000 genomes]
rs12176630	0.81[CHB][hapmap]
rs12234995	0.90[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs12541990	1.00[CEU][hapmap]
rs12543503	0.84[CEU][hapmap]
rs12546825	0.89[EUR][1000 genomes]
rs12547930	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12547969	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13250360	0.88[ASN][1000 genomes]
rs13258377	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13259064	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13262255	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs16916994	0.81[CHB][hapmap]
rs17646077	0.86[ASN][1000 genomes]
rs17718793	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs34759911	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35184808	0.90[EUR][1000 genomes]
rs4377930	0.82[YRI][hapmap]
rs4478541	0.82[YRI][hapmap]
rs4644204	0.88[ASN][1000 genomes]
rs4735322	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4735324	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4735325	0.81[YRI][hapmap]
rs6471483	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6471491	0.82[YRI][hapmap]
rs66831269	0.90[EUR][1000 genomes]
rs6985400	0.81[YRI][hapmap]
rs7386109	0.83[ASN][1000 genomes]
rs7387701	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7813205	0.84[EUR][1000 genomes]
rs7824039	0.86[EUR][1000 genomes]
rs7826057	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7840896	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv532338	chr8:95296118-95971825	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95733000-95803800	Weak transcription	Psoas Muscle	Psoas
2	chr8:95733000-95805200	Weak transcription	Colonic Mucosa	Colon
3	chr8:95733200-95805000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr8:95733600-95809400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr8:95733800-95806400	Weak transcription	Fetal Brain Male	brain
6	chr8:95740800-95799000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr8:95752400-95809200	Weak transcription	NHLF	lung
8	chr8:95752600-95805600	Weak transcription	NHEK	skin
9	chr8:95761800-95803600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr8:95773200-95804800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr8:95773600-95809400	Weak transcription	HSMMtube	muscle
12	chr8:95773800-95802600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr8:95774000-95798000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:95774800-95799800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr8:95774800-95803200	Weak transcription	Fetal Heart	heart
16	chr8:95776200-95797800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr8:95776200-95803800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr8:95777400-95804000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr8:95778600-95802600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr8:95780800-95808000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr8:95781200-95800800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr8:95783400-95798000	Strong transcription	Osteobl	bone
23	chr8:95784200-95801200	Weak transcription	Brain Germinal Matrix	brain
24	chr8:95785000-95796200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:95785000-95799400	Weak transcription	Brain Substantia Nigra	brain
26	chr8:95785000-95802400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:95785000-95803800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr8:95785000-95804600	Weak transcription	Right Ventricle	heart
29	chr8:95785000-95809800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr8:95785200-95803200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:95785200-95805000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr8:95785800-95809200	Weak transcription	Colon Smooth Muscle	Colon
33	chr8:95786200-95803800	Weak transcription	Small Intestine	intestine
34	chr8:95786200-95811600	Weak transcription	Spleen	Spleen
35	chr8:95786200-95812800	Weak transcription	Gastric	stomach
36	chr8:95786400-95809600	Weak transcription	Lung	lung
37	chr8:95786600-95802400	Weak transcription	Esophagus	oesophagus
38	chr8:95786600-95807800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr8:95786800-95796600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr8:95789200-95804400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:95789400-95796000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr8:95789400-95799200	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr8:95789600-95796400	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr8:95789600-95797800	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr8:95789600-95797800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr8:95789600-95798000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:95789600-95798000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:95789600-95804400	Strong transcription	Liver	Liver
49	chr8:95789800-95798000	Strong transcription	Adipose Nuclei	Adipose
50	chr8:95790200-95797400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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