Variant report

Variant	rs2952345
Chromosome Location	chr2:183935867-183935868
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10183561	1.00[JPT][hapmap]
rs11676029	0.81[AFR][1000 genomes]
rs1606994	0.92[AFR][1000 genomes]
rs16823717	1.00[JPT][hapmap]
rs16823721	1.00[JPT][hapmap]
rs16823967	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs16823970	1.00[JPT][hapmap]
rs16823971	1.00[JPT][hapmap]
rs16823974	1.00[JPT][hapmap]
rs16823976	1.00[JPT][hapmap]
rs16824001	1.00[JPT][hapmap]
rs2675114	1.00[MEX][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2675115	0.82[CEU][hapmap];0.94[GIH][hapmap];1.00[MEX][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2675116	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2675117	0.82[JPT][hapmap];0.80[ASN][1000 genomes]
rs2944346	1.00[JPT][hapmap]
rs3748879	1.00[JPT][hapmap]
rs4666607	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs925805	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1005281	chr2:183803173-184093877	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv875485	chr2:183827018-184195265	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1010799	chr2:183855680-184244721	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv536072	chr2:183855680-184244721	Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv1003519	chr2:183885544-184015868	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr2:183934800-183943000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:183934800-183943000	Weak transcription	Esophagus	oesophagus
3	chr2:183934800-183943000	Weak transcription	Right Atrium	heart
4	chr2:183935600-183936200	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr2:183935600-183936400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr2:183935600-183936400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr2:183935600-183936600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr2:183935600-183937200	Enhancers	Pancreas	Pancrea
9	chr2:183935800-183936200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:183935800-183936200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr2:183935800-183936200	Flanking Active TSS	HepG2	liver
12	chr2:183935800-183936400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:183935800-183936400	Enhancers	Gastric	stomach
14	chr2:183935800-183936600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:183935800-183943000	Weak transcription	Aorta	Aorta

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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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