Variant report

Variant	rs62326841
Chromosome Location	chr4:119852744-119852745
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10021334	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11098462	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17050270	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17050285	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28542234	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57021447	0.84[EUR][1000 genomes]
rs62326836	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7349616	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs736692	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs736693	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs736694	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7654417	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7661292	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7676506	0.97[EUR][1000 genomes];0.91[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	chr4:119851600-119852800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr4:119851800-119853600	Weak transcription	Colon Smooth Muscle	Colon
15	chr4:119852200-119857000	Weak transcription	Ovary	ovary

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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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