Variant report

Variant	rs377096416
Chromosome Location	chr2:152496885-152496886
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934136	chr2:152308156-152664443	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1005746	chr2:152361972-153059840	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv535984	chr2:152361972-153059840	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv2974	chr2:152401495-152499455	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv469804	chr2:152404429-152570882	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv482520	chr2:152404429-152570882	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv961518	chr2:152496377-152497078	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152482000-152502400	Strong transcription	Fetal Muscle Leg	muscle
2	chr2:152482000-152507600	Strong transcription	Fetal Muscle Trunk	muscle
3	chr2:152488600-152499400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:152489600-152505200	Strong transcription	HSMMtube	muscle
5	chr2:152492000-152504000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:152492000-152506800	Weak transcription	Psoas Muscle	Psoas
7	chr2:152492400-152497000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
8	chr2:152494400-152497000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr2:152494400-152497200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr2:152495000-152501800	Weak transcription	Right Ventricle	heart
11	chr2:152495200-152497200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr2:152495200-152500000	Strong transcription	Skeletal Muscle Female	skeletal muscle
13	chr2:152495200-152502400	Weak transcription	Aorta	Aorta
14	chr2:152495400-152497000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr2:152495600-152497000	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr2:152496000-152497800	Weak transcription	HepG2	liver
17	chr2:152496400-152497200	Enhancers	Primary T cells fromperipheralblood	blood
18	chr2:152496400-152497200	Enhancers	Primary Natural Killer cells 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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