Variant report

Variant	rs13225141
Chromosome Location	chr7:118279901-118279902
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10235550	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10953871	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1120921	0.82[EUR][1000 genomes]
rs1120922	0.82[EUR][1000 genomes]
rs11509197	0.86[EUR][1000 genomes]
rs11560382	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11761992	0.81[EUR][1000 genomes]
rs11762065	0.82[EUR][1000 genomes]
rs11767676	0.81[EUR][1000 genomes]
rs11771057	0.86[EUR][1000 genomes]
rs12706196	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13241168	0.95[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1355314	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1397325	0.82[EUR][1000 genomes]
rs1510502	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1510504	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1606005	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1721228	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1880152	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1916710	0.92[AMR][1000 genomes]
rs1916716	0.81[EUR][1000 genomes]
rs1996945	0.81[EUR][1000 genomes]
rs2030649	0.86[EUR][1000 genomes]
rs2049368	0.86[EUR][1000 genomes]
rs2063370	0.86[EUR][1000 genomes]
rs2175297	0.86[EUR][1000 genomes]
rs2175298	0.87[EUR][1000 genomes]
rs2175299	0.86[EUR][1000 genomes]
rs2214150	0.82[EUR][1000 genomes]
rs2248782	0.82[EUR][1000 genomes]
rs2521214	0.82[EUR][1000 genomes]
rs2521215	0.82[EUR][1000 genomes]
rs2521216	0.82[EUR][1000 genomes]
rs2521217	0.82[EUR][1000 genomes]
rs2665760	0.82[EUR][1000 genomes]
rs2665763	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2665764	0.82[EUR][1000 genomes]
rs2665765	0.82[EUR][1000 genomes]
rs2665766	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2665769	0.82[EUR][1000 genomes]
rs2665770	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2689753	0.82[EUR][1000 genomes]
rs2689754	0.82[EUR][1000 genomes]
rs2689755	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2689756	0.81[EUR][1000 genomes]
rs2689757	0.82[EUR][1000 genomes]
rs2689758	0.82[EUR][1000 genomes]
rs304513	0.81[EUR][1000 genomes]
rs304514	0.81[EUR][1000 genomes]
rs304521	0.89[AMR][1000 genomes]
rs304524	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs304525	0.81[EUR][1000 genomes]
rs304534	0.95[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs304535	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4730879	0.86[EUR][1000 genomes]
rs55698509	0.86[EUR][1000 genomes]
rs56141723	0.86[EUR][1000 genomes]
rs57668449	0.86[EUR][1000 genomes]
rs58071836	0.86[EUR][1000 genomes]
rs58152297	0.86[EUR][1000 genomes]
rs62470082	0.86[EUR][1000 genomes]
rs62470083	0.86[EUR][1000 genomes]
rs62470084	0.85[EUR][1000 genomes]
rs62470086	0.86[EUR][1000 genomes]
rs62470087	0.87[EUR][1000 genomes]
rs6466671	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6949669	0.86[EUR][1000 genomes]
rs6951273	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6967347	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6972496	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs778876	0.86[EUR][1000 genomes]
rs7796854	0.81[EUR][1000 genomes]
rs7800988	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs960884	0.86[EUR][1000 genomes]
rs960886	0.86[EUR][1000 genomes]
rs9641606	0.86[EUR][1000 genomes]
rs9641607	0.85[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118270400-118280400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:118271800-118280600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr7:118273200-118280400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr7:118275800-118280400	Weak transcription	HUES64 Cell Line	embryonic stem cell

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