Variant report

Variant	rs10885934
Chromosome Location	chr10:118198270-118198271
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10885932	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10885935	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11197681	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12415255	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17094693	0.83[ASN][1000 genomes]
rs17094710	0.83[ASN][1000 genomes]
rs17094717	0.83[ASN][1000 genomes]
rs17094724	0.83[ASN][1000 genomes]
rs17094739	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17094741	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs17094744	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs17094748	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs17107883	0.83[ASN][1000 genomes]
rs57823536	0.83[ASN][1000 genomes]
rs58682643	0.83[ASN][1000 genomes]
rs62619836	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832001	chr10:118138370-118315059	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv948195	chr10:118198121-118199888	Strong transcription Genic enhancers Weak transcription	TF binding region	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	chr10:118191600-118216200	Weak transcription	Pancreas	Pancrea
2	chr10:118197000-118199200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr10:118197000-118199600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr10:118197200-118199400	Strong transcription	NHEK	skin
5	chr10:118197800-118199200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr10:118198000-118199000	Strong transcription	HMEC	breast

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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