Variant report

Variant	rs11130091
Chromosome Location	chr3:46504531-46504532
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1042073	0.80[CEU][hapmap]
rs1126478	0.80[CEU][hapmap]
rs11707471	0.80[CEU][hapmap]
rs11716497	0.84[CEU][hapmap]
rs17141154	0.84[AFR][1000 genomes]
rs4234463	0.80[CEU][hapmap]
rs4683234	0.80[CEU][hapmap]
rs6441990	0.80[CEU][hapmap]
rs6441992	0.80[CEU][hapmap]
rs6776504	0.80[CEU][hapmap]
rs6794622	0.80[CEU][hapmap]
rs743659	0.80[CEU][hapmap]
rs9862186	1.00[CEU][hapmap];0.87[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9862388	0.80[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014624	chr3:46463424-46549188	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
2	nsv1013306	chr3:46469014-46698538	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers 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 target site	10 gene(s)	inside rSNPs	diseases
3	nsv1009892	chr3:46496775-46546918	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv536553	chr3:46496775-46546918	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46498000-46504800	Weak transcription	Pancreas	Pancrea
2	chr3:46503200-46504800	Enhancers	Primary B cells from cord blood	blood
3	chr3:46503800-46506800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr3:46504000-46504800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr3:46504000-46504800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
6	chr3:46504000-46505000	Enhancers	Right Atrium	heart
7	chr3:46504000-46505200	Active TSS	Left Ventricle	heart
8	chr3:46504000-46506800	Bivalent Enhancer	Fetal Muscle Leg	muscle
9	chr3:46504000-46506800	Enhancers	Lung	lung
10	chr3:46504200-46504600	Bivalent Enhancer	Fetal Intestine Small	intestine
11	chr3:46504200-46504600	Active TSS	Right Ventricle	heart
12	chr3:46504200-46505400	Enhancers	HUVEC	blood vessel
13	chr3:46504200-46506800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr3:46504400-46504600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
15	chr3:46504400-46504600	Bivalent Enhancer	Stomach Mucosa	stomach
16	chr3:46504400-46504800	Flanking Active TSS	Spleen	Spleen
17	chr3:46504400-46505000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
18	chr3:46504400-46505400	Weak transcription	Gastric	stomach

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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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