Variant report

Variant	rs16826289
Chromosome Location	chr3:156190375-156190376
allele	A/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:15)

rs_ID	r²[population]
rs13315111	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13315136	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13323374	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16826288	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41267915	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58374771	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6770093	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6777276	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6801966	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73023974	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73873389	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7629988	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7641703	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7648656	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9841854	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014755	chr3:155889430-156411894	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv829764	chr3:156174824-156347774	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
3	nsv877683	chr3:156180366-156272351	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156174800-156192600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:156183400-156200400	Weak transcription	HSMM	muscle
3	chr3:156187800-156200800	Weak transcription	HSMMtube	muscle
4	chr3:156189000-156190600	Weak transcription	Fetal Stomach	stomach
5	chr3:156189200-156190800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr3:156189200-156190800	Enhancers	K562	blood
7	chr3:156189200-156191800	Enhancers	Rectal Smooth Muscle	rectum
8	chr3:156189400-156191400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr3:156189600-156192600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:156189800-156190800	Enhancers	Fetal Muscle Leg	muscle
11	chr3:156190000-156194600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr3:156190000-156195200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr3:156190000-156202400	Weak transcription	Aorta	Aorta
14	chr3:156190200-156191400	Enhancers	Colon Smooth Muscle	Colon

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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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