Variant report

Variant	rs545766098
Chromosome Location	chr3:156926237-156926238
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829766	chr3:156811536-157020551	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv877687	chr3:156924793-157044184	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr3:156919400-156929000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr3:156919600-156928800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr3:156920200-156929600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr3:156923000-156927400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr3:156923400-156926400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:156923400-156927400	Weak transcription	Fetal Stomach	stomach
7	chr3:156923400-156928600	Weak transcription	Colon Smooth Muscle	Colon
8	chr3:156923800-156928400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:156924400-156934000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr3:156925000-156929200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:156925400-156927000	Weak transcription	Primary T cells from cord blood	blood
12	chr3:156925600-156928000	Weak transcription	Pancreas	Pancrea
13	chr3:156926000-156926600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr3:156926200-156928600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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Input of quick search could be:

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

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