Variant report

Variant	rs57537546
Chromosome Location	chr7:140009662-140009663
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889247	chr7:139855216-140033631	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1026255	chr7:139944473-140043299	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv517812	chr7:140009332-140010108	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140003400-140010000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:140004600-140010200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr7:140004600-140011200	Enhancers	HepG2	liver
4	chr7:140004600-140015400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr7:140006000-140015400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:140007000-140011600	Weak transcription	Primary B cells from cord blood	blood
7	chr7:140007400-140010800	Enhancers	Ovary	ovary
8	chr7:140008400-140010000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:140008400-140014800	Weak transcription	Stomach Mucosa	stomach
10	chr7:140008800-140010400	Enhancers	Colon Smooth Muscle	Colon
11	chr7:140008800-140012200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr7:140009200-140010200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr7:140009200-140010800	Enhancers	A549	lung
14	chr7:140009400-140014800	Weak transcription	Colonic Mucosa	Colon
15	chr7:140009400-140015000	Enhancers	Primary monocytes fromperipheralblood	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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