Variant report

Variant	rs72660502
Chromosome Location	chr1:56806209-56806210
allele	C/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:41)

rs_ID	r²[population]
rs11799457	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11803744	0.83[ASN][1000 genomes]
rs11809768	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11811596	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12064855	0.91[ASN][1000 genomes]
rs12067784	0.91[ASN][1000 genomes]
rs12090289	0.91[ASN][1000 genomes]
rs12097108	0.91[ASN][1000 genomes]
rs12563026	0.91[ASN][1000 genomes]
rs12564902	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12566405	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12567265	0.91[ASN][1000 genomes]
rs12569169	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34846848	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs55791695	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55896510	0.83[ASN][1000 genomes]
rs56061713	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56067074	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56164989	1.00[ASN][1000 genomes]
rs57024161	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60307274	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6666711	0.83[ASN][1000 genomes]
rs72660490	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72660491	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72660493	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72660494	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72660496	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72660497	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72660498	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72660499	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72662204	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72662205	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72662206	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72662207	0.91[ASN][1000 genomes]
rs72662213	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72662214	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72662217	0.91[ASN][1000 genomes]
rs72662227	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72662230	0.83[ASN][1000 genomes]
rs72662232	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72662235	0.83[ASN][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	nsv1006422	chr1:56734772-56828606	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv534972	chr1:56734772-56828606	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1015037	chr1:56784322-56814739	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56791200-56820800	Weak transcription	Aorta	Aorta
2	chr1:56798400-56807800	Weak transcription	Fetal Intestine Small	intestine
3	chr1:56805000-56806600	Enhancers	Psoas Muscle	Psoas
4	chr1:56805600-56806400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:56805600-56806400	Enhancers	Fetal Muscle Leg	muscle
6	chr1:56805600-56806400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
7	chr1:56805600-56806600	Enhancers	Left Ventricle	heart
8	chr1:56805800-56806400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:56805800-56806400	Enhancers	NHDF-Ad	bronchial
10	chr1:56806200-56806400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:56806200-56806400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle

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