Variant report

Variant	rs6655947
Chromosome Location	chr1:166982719-166982720
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1041238	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10918607	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs10918608	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11578336	0.88[CHB][hapmap];0.93[JPT][hapmap]
rs11802666	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11805946	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12118335	0.99[ASN][1000 genomes]
rs12126991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12131832	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12133327	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12134016	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12145919	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12564877	0.94[ASN][1000 genomes]
rs12569084	0.88[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2296837	0.89[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2312487	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2312675	0.80[CHB][hapmap]
rs3736988	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs41269702	0.81[ASN][1000 genomes]
rs4657621	0.85[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs56093705	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61447801	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61606407	0.81[ASN][1000 genomes]
rs6427053	1.00[CHB][hapmap];0.86[JPT][hapmap];0.97[ASN][1000 genomes]
rs6660048	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs6661553	0.88[CEU][hapmap];0.97[YRI][hapmap]
rs6662130	0.91[ASN][1000 genomes]
rs6665341	0.81[ASN][1000 genomes]
rs6667210	0.96[CEU][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs6669886	0.87[CHB][hapmap];0.93[JPT][hapmap]
rs6673622	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6673720	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6681562	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6681571	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6682062	0.81[ASN][1000 genomes]
rs6694465	0.92[CEU][hapmap];0.97[YRI][hapmap];0.85[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs6695162	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs6695609	0.88[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6696203	0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6697417	0.83[ASN][1000 genomes]
rs6698931	0.85[YRI][hapmap]
rs6699159	0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7511933	0.91[ASN][1000 genomes]
rs7518155	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs7528849	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs7533688	0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7545911	0.88[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7550698	0.81[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	nsv1004148	chr1:166951869-167016311	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2750815	chr1:166953866-167180342	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166980400-166985000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:166980400-166985400	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr1:166980800-166985200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr1:166982200-166982800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:166982200-166983200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr1:166982200-166983200	Enhancers	HMEC	breast
7	chr1:166982400-166982800	Enhancers	NHEK	skin
8	chr1:166982400-166983000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:166982400-166983200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr1:166982400-166983400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:166982400-166983400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:166982600-166983200	Enhancers	HUES64 Cell Line	embryonic stem cell

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