Variant report

Variant	rs10216198
Chromosome Location	chr7:103662959-103662960
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103659260..103661864-chr7:103662623..103664165,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10216187	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10224925	0.99[ASN][1000 genomes]
rs10230068	0.99[ASN][1000 genomes]
rs10273035	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10487182	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11971265	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11972170	0.83[EUR][1000 genomes]
rs12056044	0.89[ASN][1000 genomes]
rs17158113	0.99[ASN][1000 genomes]
rs17158137	0.99[ASN][1000 genomes]
rs17158144	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17158288	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55825925	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56272143	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56334899	0.83[EUR][1000 genomes]
rs60375583	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6465955	0.99[ASN][1000 genomes]
rs6465957	0.99[ASN][1000 genomes]
rs71154387	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73405684	0.83[EUR][1000 genomes]
rs73405688	0.83[EUR][1000 genomes]
rs73405690	0.83[EUR][1000 genomes]
rs73405692	0.83[EUR][1000 genomes]
rs73409925	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73409927	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][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	nsv888924	chr7:103637906-103706936	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 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	chr7:103662400-103663000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:103662400-103663800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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