Variant report

Variant	rs10494211
Chromosome Location	chr1:119193131-119193132
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1213857	0.93[CHB][hapmap];0.89[JPT][hapmap];0.94[ASN][1000 genomes]
rs3863757	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3903912	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4633275	0.93[CHB][hapmap];0.91[JPT][hapmap];0.94[ASN][1000 genomes]
rs58780415	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60134893	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73003504	0.97[ASN][1000 genomes]
rs73003506	0.97[ASN][1000 genomes]
rs73003509	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73003531	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73005259	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73005266	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7533117	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7543320	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7543613	0.91[EUR][1000 genomes];0.97[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	esv3494191	chr1:118772550-119719548	Enhancers Strong transcription Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	esv3494192	chr1:118772550-119719548	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 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	chr1:119190800-119194200	Enhancers	Fetal Heart	heart
2	chr1:119191800-119193600	Enhancers	Colon Smooth Muscle	Colon
3	chr1:119192000-119194200	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr1:119192600-119193800	Enhancers	Rectal Smooth Muscle	rectum
5	chr1:119192800-119193200	Active TSS	Skeletal Muscle Female	skeletal muscle
6	chr1:119192800-119193400	Enhancers	Fetal Muscle Leg	muscle

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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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