Variant report

Variant	rs3111223
Chromosome Location	chr1:211342486-211342487
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1338352	0.83[CHB][hapmap];0.91[CHD][hapmap];0.83[JPT][hapmap];0.92[ASN][1000 genomes]
rs1338354	0.91[ASN][1000 genomes]
rs1338355	0.91[ASN][1000 genomes]
rs1416066	0.91[ASN][1000 genomes]
rs1577986	0.90[ASN][1000 genomes]
rs1591746	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2066025	0.80[ASN][1000 genomes]
rs2211040	0.90[ASN][1000 genomes]
rs3111222	0.92[ASN][1000 genomes]
rs3120779	0.95[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3811393	0.80[ASN][1000 genomes]
rs6665927	0.83[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs7548416	0.92[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	nsv945276	chr1:211341161-211348032	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211342000-211342600	Active TSS	Primary T cells from cord blood	blood
2	chr1:211342400-211342600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:211342400-211342800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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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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