Variant report

Variant	rs532591038
Chromosome Location	chr7:140004103-140004104
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	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	nsv824319	chr7:140004029-140009178	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv442070	chr7:140004043-140008466	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:139986800-140007800	Weak transcription	Fetal Intestine Small	intestine
2	chr7:139999600-140008800	Weak transcription	Colonic Mucosa	Colon
3	chr7:139999800-140004200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr7:140000200-140004200	Enhancers	HepG2	liver
5	chr7:140003200-140006600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr7:140003200-140006800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr7:140003400-140004200	Weak transcription	Stomach Mucosa	stomach
8	chr7:140003400-140004600	Enhancers	Primary B cells from cord blood	blood
9	chr7:140003400-140010000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:140003600-140004800	Enhancers	Primary B cells from peripheral blood	blood
11	chr7:140004000-140004200	Enhancers	GM12878-XiMat	blood
12	chr7:140004000-140004400	Enhancers	Primary T cells from cord blood	blood
13	chr7:140004000-140004600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr7:140004000-140004600	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr7:140004000-140004600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr7:140004000-140005000	Enhancers	Primary Natural Killer 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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