Variant report

Variant	rs10075691
Chromosome Location	chr5:97963948-97963949
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10038064	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10038307	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10039819	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10043199	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10045612	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10059259	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10065249	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10068399	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10479181	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10479183	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11242242	1.00[ASN][1000 genomes]
rs11242255	1.00[ASN][1000 genomes]
rs11950934	0.94[ASN][1000 genomes]
rs13361670	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1421633	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1421634	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs149126	0.88[ASN][1000 genomes]
rs152960	0.83[ASN][1000 genomes]
rs152964	0.83[ASN][1000 genomes]
rs154201	0.88[ASN][1000 genomes]
rs154203	0.88[ASN][1000 genomes]
rs154204	0.88[ASN][1000 genomes]
rs17166201	0.94[ASN][1000 genomes]
rs17661925	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs187385	0.83[ASN][1000 genomes]
rs2080994	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2112145	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs245444	0.88[ASN][1000 genomes]
rs27023	0.88[ASN][1000 genomes]
rs27025	0.83[ASN][1000 genomes]
rs27027	0.81[ASN][1000 genomes]
rs27032	0.83[ASN][1000 genomes]
rs27576	0.88[ASN][1000 genomes]
rs27577	0.88[ASN][1000 genomes]
rs27787	0.83[ASN][1000 genomes]
rs28079	0.83[ASN][1000 genomes]
rs29662	0.83[ASN][1000 genomes]
rs36767	0.88[ASN][1000 genomes]
rs387158	0.88[ASN][1000 genomes]
rs3907829	0.83[ASN][1000 genomes]
rs3909494	1.00[ASN][1000 genomes]
rs398955	0.83[ASN][1000 genomes]
rs40175	0.90[ASN][1000 genomes]
rs4277375	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs457225	0.88[ASN][1000 genomes]
rs463314	0.88[ASN][1000 genomes]
rs464686	0.88[ASN][1000 genomes]
rs465312	0.88[ASN][1000 genomes]
rs467627	0.88[ASN][1000 genomes]
rs467657	0.88[ASN][1000 genomes]
rs468016	0.88[ASN][1000 genomes]
rs59126397	0.89[EUR][1000 genomes]
rs6883625	0.94[ASN][1000 genomes]
rs6895508	1.00[ASN][1000 genomes]
rs73149511	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7444475	0.83[ASN][1000 genomes]

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	nsv1016611	chr5:97873846-98035559	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv537816	chr5:97873846-98035559	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv1029509	chr5:97888644-98040172	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv882413	chr5:97918829-98022320	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1832089	chr5:97934125-97976039	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97946400-97967200	Weak transcription	HSMMtube	muscle
2	chr5:97956600-97964400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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