Variant report

Variant	rs73029179
Chromosome Location	chr2:182051427-182051428
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs56977169	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs59260686	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62180166	0.92[ASN][1000 genomes]
rs73025698	0.96[ASN][1000 genomes]
rs73027403	0.96[ASN][1000 genomes]
rs73027409	0.96[ASN][1000 genomes]
rs73027412	0.96[ASN][1000 genomes]
rs73027417	0.96[ASN][1000 genomes]
rs73027433	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027437	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027439	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027441	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027445	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027455	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027457	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027466	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027468	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027474	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027482	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73027499	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73027502	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73029106	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73029172	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73029178	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73029181	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73029183	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73029186	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73029188	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73976816	0.92[ASN][1000 genomes]
rs997716	0.96[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	nsv431824	chr2:181946115-182118559	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182043800-182053200	Weak transcription	Primary T cells from cord blood	blood
2	chr2:182044000-182054400	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr2:182044000-182055400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr2:182045000-182053400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr2:182045000-182053600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr2:182045400-182062000	Weak transcription	Dnd41	blood
7	chr2:182049000-182054400	Weak transcription	Fetal Thymus	thymus
8	chr2:182049200-182055400	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr2:182050400-182051600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr2:182050800-182051600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:182050800-182053600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:182050800-182054200	Weak transcription	HSMM	muscle
13	chr2:182050800-182063400	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr2:182051000-182053400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr2:182051200-182054200	Weak transcription	HSMMtube	muscle

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