Variant report

Variant	rs4975719
Chromosome Location	chr5:2010162-2010163
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10043083	0.82[EUR][1000 genomes]
rs1023980	0.82[CHB][hapmap]
rs1023981	0.81[CHB][hapmap]
rs10462750	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10474733	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10474734	0.85[EUR][1000 genomes]
rs1552435	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16902318	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16902321	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2129471	0.88[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2129472	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28392808	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3902820	0.81[EUR][1000 genomes]
rs4074914	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4246753	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4246754	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4254943	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4314451	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4398675	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4398680	0.84[EUR][1000 genomes]
rs4413568	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4463207	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4505990	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4526149	0.82[EUR][1000 genomes]
rs4975786	0.85[EUR][1000 genomes]
rs4975794	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4975795	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4975796	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4975797	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4975798	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4975802	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61177713	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6867032	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7729761	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9312970	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9312971	0.82[CHB][hapmap]

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	nsv817407	chr5:1495354-2191460	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
2	nsv869236	chr5:1719263-2259100	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
3	nsv915846	chr5:1891098-2167677	Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1026930	chr5:1898993-2126061	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv427705	chr5:1950467-2115059	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:2007400-2011800	Enhancers	Fetal Heart	heart
2	chr5:2008600-2012000	Weak transcription	Right Atrium	heart
3	chr5:2008800-2010200	Bivalent Enhancer	Fetal Muscle Leg	muscle
4	chr5:2008800-2010400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
5	chr5:2008800-2011600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:2008800-2013200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:2009000-2011800	Weak transcription	NHEK	skin
8	chr5:2009000-2013200	Weak transcription	HMEC	breast
9	chr5:2009200-2010800	Enhancers	Dnd41	blood
10	chr5:2009200-2011600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:2009400-2011200	Weak transcription	Left Ventricle	heart
12	chr5:2009400-2012000	Weak transcription	Right Ventricle	heart
13	chr5:2009400-2014400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:2009600-2010200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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