Variant report

Variant	rs1792585
Chromosome Location	chr11:15201645-15201646
allele	C/T
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:10)

rs_ID	r²[population]
rs1573545	0.83[ASN][1000 genomes]
rs1624731	0.80[ASN][1000 genomes]
rs1714375	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1714382	0.80[ASN][1000 genomes]
rs1792529	0.80[ASN][1000 genomes]
rs1792586	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1792587	0.86[ASN][1000 genomes]
rs1945596	0.80[ASN][1000 genomes]
rs2679634	0.94[ASN][1000 genomes]
rs3110501	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038154	chr11:14991411-15246500	Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv540950	chr11:14991411-15246500	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv897007	chr11:14991411-15260124	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv530217	chr11:14991411-15275034	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2830370	chr11:15142247-15444094	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1036474	chr11:15181521-15209506	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15197600-15211600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:15197800-15221000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:15199000-15203200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:15200000-15202600	Enhancers	NHDF-Ad	bronchial
5	chr11:15200200-15202000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:15200200-15202200	Enhancers	HSMM	muscle
7	chr11:15200400-15202600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:15200600-15202000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:15200600-15202200	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr11:15201000-15202200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:15201000-15202200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:15201000-15202200	Enhancers	Aorta	Aorta
13	chr11:15201200-15202200	Enhancers	GM12878-XiMat	blood
14	chr11:15201200-15218800	Weak transcription	Fetal Brain Male	brain
15	chr11:15201400-15202400	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr11:15201400-15202600	Weak transcription	Osteobl	bone
17	chr11:15201400-15207600	Weak transcription	Muscle Satellite Cultured Cells	--

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