Variant report

Variant	rs1991437
Chromosome Location	chr12:104077524-104077525
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12422614	1.00[AFR][1000 genomes]
rs17034363	0.92[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17034372	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs17034394	1.00[CHB][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs3752877	1.00[AFR][1000 genomes]
rs56939481	0.89[EUR][1000 genomes]
rs58651958	0.87[ASN][1000 genomes]
rs7138431	1.00[CHB][hapmap];0.90[JPT][hapmap];0.85[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	nsv560038	chr12:104053420-104092996	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104074800-104077800	Weak transcription	Spleen	Spleen
2	chr12:104074800-104079000	Weak transcription	Fetal Muscle Leg	muscle
3	chr12:104074800-104089400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr12:104075000-104079400	Weak transcription	Fetal Intestine Small	intestine
5	chr12:104075200-104079000	Weak transcription	Fetal Intestine Large	intestine

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

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