Variant report

Variant	rs73026084
Chromosome Location	chr2:168440669-168440670
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10182563	0.84[AFR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10182569	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10188352	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10195156	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10196108	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1079438	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1079439	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10930274	0.83[ASN][1000 genomes]
rs11686950	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1227106	0.81[EUR][1000 genomes]
rs1227123	0.84[ASN][1000 genomes]
rs1237905	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13398335	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13427510	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1367918	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1367921	0.88[ASN][1000 genomes]
rs1431896	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1431903	0.87[EUR][1000 genomes]
rs1615054	0.80[ASN][1000 genomes]
rs1617451	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1653383	0.81[EUR][1000 genomes]
rs1653432	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1730715	0.80[EUR][1000 genomes]
rs1730726	0.84[EUR][1000 genomes]
rs1835745	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2464039	0.80[EUR][1000 genomes]
rs4667958	0.80[EUR][1000 genomes]
rs6743050	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73013367	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73013383	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs734283	0.80[EUR][1000 genomes]
rs734284	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs735424	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7576381	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7590728	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs891741	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs891742	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491872	chr2:168220323-168737986	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv834449	chr2:168340043-168511856	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv583592	chr2:168356232-168721539	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1008206	chr2:168401249-168452887	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv528466	chr2:168402224-168447851	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv583593	chr2:168402224-168452630	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv1004326	chr2:168403386-168452887	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168439600-168440800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:168439600-168441000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr2:168439600-168441000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr2:168439800-168441000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr2:168439800-168441000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:168439800-168441000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr2:168439800-168448400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:168440400-168441200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:168440600-168448600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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