Variant report

Variant	rs7796197
Chromosome Location	chr7:96946524-96946525
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1012107	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1012108	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11762100	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12538699	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1420167	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1420168	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1420169	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1420170	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1420171	0.83[ASN][1000 genomes]
rs1420172	0.83[ASN][1000 genomes]
rs2107598	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2394621	0.83[ASN][1000 genomes]
rs34212633	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34597458	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35748713	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35955969	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36003653	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3944117	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4727359	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4729350	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62499531	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62500784	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62500785	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62500787	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6465578	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6947667	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6967969	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7455701	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7455772	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7779114	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7796040	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7796251	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7796739	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9691916	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[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	nsv1028319	chr7:96940309-97012717	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv274910	chr7:96946369-96968328	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2762689	chr7:96946381-96946699	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96943800-96947000	Weak transcription	H9 Cell Line	embryonic stem cell

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