Variant report

Variant	rs9492879
Chromosome Location	chr6:131565463-131565464
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs9321278	0.83[AFR][1000 genomes]
rs9483229	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9483230	1.00[YRI][hapmap]
rs9492856	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs9492859	0.88[AFR][1000 genomes]
rs9492866	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9492867	0.94[AFR][1000 genomes]
rs9492871	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9492882	1.00[AFR][1000 genomes]
rs9492884	1.00[YRI][hapmap];1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032955	chr6:131298803-131818502	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538443	chr6:131298803-131818502	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv830807	chr6:131390952-131581931	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv886664	chr6:131443843-131754930	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv886665	chr6:131518894-131611309	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
6	nsv830808	chr6:131521115-131735320	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
7	esv1835599	chr6:131554291-131590766	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131543000-131571200	Weak transcription	Adipose Nuclei	Adipose
2	chr6:131546600-131565600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr6:131546600-131566000	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr6:131559800-131571200	Weak transcription	Liver	Liver
5	chr6:131562600-131570800	Weak transcription	Primary T cells from cord blood	blood
6	chr6:131562600-131571200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:131562600-131571400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:131563000-131580000	Weak transcription	Small Intestine	intestine
9	chr6:131564000-131565600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr6:131564000-131565800	Enhancers	Fetal Heart	heart
11	chr6:131564400-131565600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr6:131564600-131570600	Weak transcription	Fetal Brain Male	brain
13	chr6:131564600-131571200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr6:131564800-131571200	Weak transcription	Brain Hippocampus Middle	brain
15	chr6:131565000-131566800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr6:131565200-131565600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:131565200-131565800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:131565200-131565800	Genic enhancers	Left Ventricle	heart
19	chr6:131565200-131565800	Enhancers	NHEK	skin
20	chr6:131565200-131566000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:131565200-131566600	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr6:131565200-131567200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:131565400-131565800	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr6:131565400-131566000	Enhancers	HMEC	breast
25	chr6:131565400-131567200	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr6:131565400-131571000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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