Variant report

Variant	rs7801037
Chromosome Location	chr7:18897511-18897512
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10230371	0.84[EUR][1000 genomes]
rs10237149	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10237280	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10237366	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10270210	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10486314	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11761877	0.88[ASN][1000 genomes]
rs12530943	0.82[AMR][1000 genomes]
rs12536081	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12536836	0.85[EUR][1000 genomes]
rs12699994	0.94[ASN][1000 genomes]
rs12699998	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12699999	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12700000	0.90[ASN][1000 genomes]
rs12700001	0.82[EUR][1000 genomes]
rs12700002	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12700003	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13233322	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13242358	0.88[ASN][1000 genomes]
rs13242758	0.82[AMR][1000 genomes]
rs13245206	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2028015	0.87[ASN][1000 genomes]
rs2249817	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2286213	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs34854568	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55761404	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59987684	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60976379	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6461387	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6461389	0.82[AMR][1000 genomes]
rs6461390	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6461391	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6461392	0.88[AMR][1000 genomes]
rs6461393	0.81[AMR][1000 genomes]
rs6461394	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs67248060	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6951144	0.87[AMR][1000 genomes]
rs6951745	0.89[AMR][1000 genomes]
rs6973029	0.82[AMR][1000 genomes]
rs756854	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7794241	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498112	chr7:18677922-18991946	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv887813	chr7:18720135-18995552	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv523497	chr7:18896011-18959381	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18895400-18902800	Weak transcription	Aorta	Aorta
2	chr7:18896200-18900800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr7:18896600-18901800	Enhancers	NHDF-Ad	bronchial
4	chr7:18896800-18900600	Weak transcription	Osteobl	bone
5	chr7:18897200-18897600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:18897200-18900400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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