Variant report

Variant	rs10157798
Chromosome Location	chr1:171626941-171626942
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:171618444..171621917-chr1:171624017..171626963,3	K562	blood:
2	chr1:171625427..171627489-chr1:171632106..171634164,2	K562	blood:

Variant related genes	Relation type
ENSG00000034971	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1001373	0.82[CHD][hapmap]
rs10489248	0.95[ASN][1000 genomes]
rs10913408	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913455	1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[ASN][1000 genomes]
rs10913456	0.92[ASN][1000 genomes]
rs10913457	0.92[ASN][1000 genomes]
rs10913458	0.95[ASN][1000 genomes]
rs10913529	0.82[CHD][hapmap]
rs11576221	0.82[CHD][hapmap]
rs11799938	1.00[CHB][hapmap];0.95[CHD][hapmap];0.88[GIH][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs11799961	1.00[CHB][hapmap];0.95[CHD][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs11800109	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11800358	0.87[ASN][1000 genomes]
rs11801712	0.87[ASN][1000 genomes]
rs11809518	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11809796	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11811408	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11811876	0.92[ASN][1000 genomes]
rs12145527	1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs12145593	0.92[ASN][1000 genomes]
rs15655	0.82[CHD][hapmap]
rs16864740	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1894664	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2014613	0.95[ASN][1000 genomes]
rs34324629	0.83[ASN][1000 genomes]
rs56941416	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56994188	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57689480	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58035845	0.92[ASN][1000 genomes]
rs59146152	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60554980	0.92[ASN][1000 genomes]
rs6662126	0.92[ASN][1000 genomes]
rs6667559	0.82[CHD][hapmap]
rs6684567	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6703259	0.89[ASN][1000 genomes]
rs73041958	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73041960	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73041965	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73041966	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73041973	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7536328	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7541132	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv14617	chr1:171016086-171726961	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv3512995	chr1:171329123-171994470	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	esv3512997	chr1:171329123-171994470	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	esv12447	chr1:171556291-171726822	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv872544	chr1:171616822-171654968	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr1:171620400-171627600	Enhancers	Fetal Muscle Leg	muscle
2	chr1:171624200-171630400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:171624600-171635200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:171624800-171629400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:171624800-171633200	Weak transcription	Psoas Muscle	Psoas
6	chr1:171625000-171627200	Enhancers	Fetal Heart	heart
7	chr1:171625000-171627400	Weak transcription	Ovary	ovary
8	chr1:171625200-171633400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr1:171625400-171632600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:171625400-171632800	Weak transcription	Right Ventricle	heart
11	chr1:171626000-171631600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:171626200-171627000	Enhancers	Fetal Stomach	stomach

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