Variant report

Variant	rs73560837
Chromosome Location	chr19:42046316-42046317
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10406890	1.00[AMR][1000 genomes]
rs10414658	1.00[AMR][1000 genomes]
rs10418236	1.00[AMR][1000 genomes]
rs10425322	1.00[AMR][1000 genomes]
rs16975289	1.00[AMR][1000 genomes]
rs73558643	1.00[AMR][1000 genomes]
rs73558647	1.00[AMR][1000 genomes]
rs73558696	1.00[AMR][1000 genomes]
rs73558697	1.00[AMR][1000 genomes]
rs73558700	1.00[AMR][1000 genomes]
rs73560806	1.00[AMR][1000 genomes]
rs73560816	1.00[AMR][1000 genomes]
rs73560817	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv510767	chr19:41962486-42049165	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv911770	chr19:41962486-42066279	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv911771	chr19:41962486-42085873	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1055515	chr19:41968797-42057334	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv911772	chr19:41985624-42066279	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv911773	chr19:42001210-42085873	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv579602	chr19:42015468-42047924	Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv978751	chr19:42036596-42073874	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42038600-42050800	Weak transcription	Spleen	Spleen
2	chr19:42042000-42046600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr19:42042200-42048400	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr19:42042200-42048600	Weak transcription	Primary T cells from cord blood	blood
5	chr19:42042200-42048600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr19:42042200-42048600	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr19:42042800-42048600	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr19:42043400-42046400	Weak transcription	GM12878-XiMat	blood
9	chr19:42043400-42052000	Weak transcription	Right Atrium	heart
10	chr19:42044800-42046400	Weak transcription	Primary B cells from cord blood	blood
11	chr19:42045000-42048400	Weak transcription	Primary B cells from peripheral blood	blood
12	chr19:42046200-42046600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr19:42046200-42047000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr19:42046200-42047000	Bivalent Enhancer	A549	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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