Variant report

Variant	rs1347703
Chromosome Location	chr4:173589490-173589491
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10016257	1.00[CHB][hapmap]
rs10026450	0.91[CEU][hapmap]
rs10029955	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10031202	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10050292	1.00[CHB][hapmap]
rs1074144	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11132960	1.00[CHB][hapmap]
rs11729518	1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11730738	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs11734921	0.85[CEU][hapmap]
rs11735233	1.00[CHB][hapmap]
rs11736072	1.00[CHB][hapmap]
rs13104048	1.00[CHB][hapmap]
rs13134091	0.84[ASN][1000 genomes]
rs13138074	1.00[CHB][hapmap]
rs13152161	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1370572	0.89[CEU][hapmap]
rs1378312	0.87[CEU][hapmap]
rs1437836	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs1437843	0.92[CEU][hapmap];1.00[CHB][hapmap];0.80[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1437844	0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1437845	1.00[CHB][hapmap];0.82[AMR][1000 genomes]
rs1437854	1.00[CHB][hapmap]
rs1437855	1.00[CHB][hapmap]
rs1437856	1.00[CHB][hapmap]
rs1455120	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1455129	0.91[CEU][hapmap]
rs1540475	1.00[CHB][hapmap]
rs1551447	0.91[CEU][hapmap]
rs1561305	1.00[CHB][hapmap]
rs1658515	0.83[CEU][hapmap]
rs17052104	1.00[CHB][hapmap]
rs17058691	0.92[CEU][hapmap];1.00[CHB][hapmap]
rs17235632	0.80[CEU][hapmap];0.87[EUR][1000 genomes]
rs2043780	1.00[CHB][hapmap]
rs2196669	0.92[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2332549	1.00[CHB][hapmap]
rs28579160	0.84[ASN][1000 genomes]
rs28727534	0.84[ASN][1000 genomes]
rs34364219	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4315754	1.00[CHB][hapmap]
rs4396969	1.00[CHB][hapmap]
rs4414931	1.00[CHB][hapmap]
rs4431209	1.00[CHB][hapmap]
rs6553639	0.92[CEU][hapmap]
rs6553640	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs67168311	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6830773	1.00[CHB][hapmap]
rs6833340	0.92[CEU][hapmap]
rs6853969	0.84[ASN][1000 genomes]
rs716645	1.00[CHB][hapmap]
rs716646	1.00[CHB][hapmap]
rs7664781	0.88[CEU][hapmap]
rs7668989	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7669486	0.84[ASN][1000 genomes]
rs7671314	0.91[CEU][hapmap]
rs7673000	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7677835	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs7691283	0.92[CEU][hapmap]
rs7692814	0.92[CEU][hapmap]
rs7693019	0.92[CEU][hapmap]
rs837189	0.81[CEU][hapmap]
rs9992901	1.00[CHB][hapmap]
rs9996298	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.91[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	nsv1031592	chr4:173112542-173662991	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv537359	chr4:173112542-173662991	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv534293	chr4:173121379-173606082	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv880685	chr4:173562564-173661711	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv880613	chr4:173569281-173661711	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173588200-173589600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:173588400-173589600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:173588800-173590000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr4:173589000-173590000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:173589000-173595400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr4:173589200-173589800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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