Variant report

Variant	rs72921369
Chromosome Location	chr1:57703608-57703609
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11800032	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11807144	1.00[ASN][1000 genomes]
rs169100	1.00[ASN][1000 genomes]
rs169101	1.00[ASN][1000 genomes]
rs17115424	1.00[ASN][1000 genomes]
rs59069448	1.00[ASN][1000 genomes]
rs59607912	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59936138	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60262534	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60349301	1.00[ASN][1000 genomes]
rs61257570	1.00[ASN][1000 genomes]
rs6675017	1.00[ASN][1000 genomes]
rs72903213	1.00[AMR][1000 genomes]
rs72903218	1.00[AMR][1000 genomes]
rs72919287	1.00[ASN][1000 genomes]
rs72921356	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57702200-57707400	Weak transcription	Fetal Intestine Large	intestine
2	chr1:57702200-57711800	Weak transcription	Fetal Intestine Small	intestine
3	chr1:57703600-57703800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:57703600-57704000	Enhancers	Lung	lung

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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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