Variant report

Variant	rs11946677
Chromosome Location	chr4:31107885-31107886
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10517226	1.00[CEU][hapmap]
rs1463841	1.00[CEU][hapmap]
rs16884400	1.00[CEU][hapmap]
rs16884408	1.00[CEU][hapmap]
rs67552245	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]

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	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1007884	chr4:31071934-31680623	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1007145	chr4:31079681-31670541	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv491749	chr4:31103307-31645668	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:31103000-31110400	Weak transcription	Ovary	ovary
2	chr4:31105400-31111000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:31106000-31111400	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:31106200-31108000	Weak transcription	Fetal Heart	heart
5	chr4:31106200-31116200	Weak transcription	Brain Germinal Matrix	brain
6	chr4:31106200-31116200	Weak transcription	Fetal Brain Male	brain
7	chr4:31106400-31108000	Weak transcription	NH-A	brain
8	chr4:31106600-31108800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:31106600-31109000	Weak transcription	Aorta	Aorta
10	chr4:31106600-31110200	Weak transcription	Fetal Lung	lung
11	chr4:31106800-31108000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr4:31107800-31110200	Enhancers	HUVEC	blood vessel

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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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