Variant report

Variant	rs4314476
Chromosome Location	chr6:161597782-161597783
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1040724	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10499315	0.83[EUR][1000 genomes]
rs10499316	0.83[EUR][1000 genomes]
rs11961712	0.83[EUR][1000 genomes]
rs13192827	0.82[EUR][1000 genomes]
rs13193634	0.84[EUR][1000 genomes]
rs13194878	0.84[EUR][1000 genomes]
rs13215186	0.83[EUR][1000 genomes]
rs13219494	0.83[EUR][1000 genomes]
rs13220357	0.83[EUR][1000 genomes]
rs16892284	0.80[EUR][1000 genomes]
rs16892303	0.84[EUR][1000 genomes]
rs17537799	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17626731	0.83[EUR][1000 genomes]
rs34620502	0.84[EUR][1000 genomes]
rs35180185	0.83[EUR][1000 genomes]
rs35267977	0.84[EUR][1000 genomes]
rs35505620	0.83[EUR][1000 genomes]
rs71565796	0.83[EUR][1000 genomes]
rs71565797	0.84[EUR][1000 genomes]
rs7744842	0.83[EUR][1000 genomes]
rs7747618	0.82[EUR][1000 genomes]
rs7751159	0.82[EUR][1000 genomes]
rs7756321	0.82[EUR][1000 genomes]
rs7758121	0.83[EUR][1000 genomes]
rs7767737	0.84[EUR][1000 genomes]
rs7770491	0.82[EUR][1000 genomes]
rs7771961	0.83[EUR][1000 genomes]
rs9458149	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv949397	chr6:161592100-161812932	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv2752091	chr6:161592100-161855785	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161585600-161626000	Weak transcription	Right Atrium	heart
2	chr6:161587400-161599600	Weak transcription	Spleen	Spleen
3	chr6:161587400-161607000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:161588000-161599800	Weak transcription	Primary T cells from cord blood	blood
5	chr6:161590000-161598800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:161590000-161611600	Weak transcription	HSMMtube	muscle
7	chr6:161590200-161607600	Weak transcription	HSMM	muscle
8	chr6:161590400-161599000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr6:161590400-161606800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:161591000-161607000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:161591400-161599200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr6:161591400-161626200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:161591600-161615400	Weak transcription	Fetal Heart	heart
14	chr6:161591800-161599200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr6:161591800-161607000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr6:161592000-161598600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:161592000-161599800	Weak transcription	Ovary	ovary
18	chr6:161592000-161607000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:161592000-161609600	Weak transcription	Fetal Brain Male	brain
20	chr6:161592200-161599200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:161592200-161602200	Weak transcription	Brain Anterior Caudate	brain
22	chr6:161592200-161606600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:161592600-161598800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:161593400-161599200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr6:161593600-161598400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:161593600-161598800	Weak transcription	Lung	lung
27	chr6:161593600-161599000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:161593600-161599600	Weak transcription	Esophagus	oesophagus

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