Variant report

Variant	rs73932877
Chromosome Location	chr19:42686873-42686874
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11880124	1.00[ASN][1000 genomes]
rs11883412	0.98[ASN][1000 genomes]
rs12232804	0.82[ASN][1000 genomes]
rs17750207	1.00[ASN][1000 genomes]
rs61088131	0.85[EUR][1000 genomes]
rs62119628	0.82[ASN][1000 genomes]
rs7248379	0.82[ASN][1000 genomes]
rs8182491	0.82[ASN][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	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv520239	chr19:42357455-42931004	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1805469	chr19:42367635-42798851	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
4	nsv911782	chr19:42514712-42931004	Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
5	esv1794508	chr19:42580026-42791462	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
6	nsv1055554	chr19:42619671-42821642	Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
7	nsv833833	chr19:42657276-42783122	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
8	nsv526186	chr19:42676481-43203507	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42681800-42703600	Weak transcription	Right Atrium	heart
2	chr19:42684200-42688400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr19:42684400-42688000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr19:42684800-42687200	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr19:42686000-42687000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr19:42686000-42687000	Enhancers	Primary hematopoietic stem cells	blood
7	chr19:42686000-42687400	Enhancers	Primary B cells from peripheral blood	blood
8	chr19:42686000-42687600	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr19:42686000-42690200	Enhancers	Primary B cells from cord blood	blood
10	chr19:42686000-42691200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr19:42686200-42687200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:42686400-42687000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr19:42686400-42687200	Enhancers	Spleen	Spleen
14	chr19:42686400-42687400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
15	chr19:42686600-42687000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:42686600-42687600	Enhancers	Primary T cells fromperipheralblood	blood
17	chr19:42686600-42690800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:42686800-42687400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
19	chr19:42686800-42688200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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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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