Variant report

Variant	rs957776
Chromosome Location	chr4:119852031-119852032
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10002822	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11726903	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12507203	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12648221	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13138512	0.89[ASN][1000 genomes]
rs1549533	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2114462	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2172013	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4611911	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4834723	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs736965	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs754397	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs875229	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[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	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv948802	chr4:119844269-120208926	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119841000-119858400	Weak transcription	Psoas Muscle	Psoas
2	chr4:119842600-119861800	Weak transcription	Right Ventricle	heart
3	chr4:119847400-119861800	Weak transcription	Left Ventricle	heart
4	chr4:119848400-119860200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr4:119848400-119861800	Weak transcription	Right Atrium	heart
6	chr4:119849400-119857200	Weak transcription	Fetal Stomach	stomach
7	chr4:119849400-119858000	Weak transcription	Aorta	Aorta
8	chr4:119849800-119857200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr4:119850200-119852800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr4:119850400-119853800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr4:119850400-119858400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr4:119851200-119860400	Weak transcription	Fetal Intestine Small	intestine
13	chr4:119851600-119852200	Enhancers	Ovary	ovary
14	chr4:119851600-119852800	Weak transcription	Rectal Smooth Muscle	rectum
15	chr4:119851800-119853600	Weak transcription	Colon Smooth Muscle	Colon

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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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