Variant report

Variant	rs3910837
Chromosome Location	chr4:33818942-33818943
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10011550	0.97[ASN][1000 genomes]
rs10021740	0.88[ASN][1000 genomes]
rs10025016	0.88[ASN][1000 genomes]
rs10030710	0.88[ASN][1000 genomes]
rs10033461	0.88[ASN][1000 genomes]
rs10033782	0.94[ASN][1000 genomes]
rs10034901	0.88[ASN][1000 genomes]
rs10050065	0.97[ASN][1000 genomes]
rs10470879	0.88[ASN][1000 genomes]
rs11945628	0.88[ASN][1000 genomes]
rs12640941	0.97[ASN][1000 genomes]
rs12642628	0.89[ASN][1000 genomes]
rs13110392	0.88[ASN][1000 genomes]
rs13111438	0.97[ASN][1000 genomes]
rs13112341	0.96[ASN][1000 genomes]
rs13113238	0.96[ASN][1000 genomes]
rs13131261	0.88[ASN][1000 genomes]
rs13136846	0.88[ASN][1000 genomes]
rs13137090	0.88[ASN][1000 genomes]
rs13139622	0.88[ASN][1000 genomes]
rs13142161	0.88[ASN][1000 genomes]
rs13142365	0.88[ASN][1000 genomes]
rs13147878	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13150067	0.88[ASN][1000 genomes]
rs1373494	0.97[ASN][1000 genomes]
rs1378039	0.88[ASN][1000 genomes]
rs1444377	0.88[ASN][1000 genomes]
rs1444378	0.88[ASN][1000 genomes]
rs1596581	0.88[ASN][1000 genomes]
rs16989167	0.87[ASN][1000 genomes]
rs16989187	0.88[ASN][1000 genomes]
rs16989190	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16995875	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2120677	0.94[ASN][1000 genomes]
rs2166108	0.94[ASN][1000 genomes]
rs2166109	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2166110	0.98[ASN][1000 genomes]
rs2338361	0.97[ASN][1000 genomes]
rs28394002	0.94[ASN][1000 genomes]
rs28489645	0.89[ASN][1000 genomes]
rs28558465	0.88[ASN][1000 genomes]
rs28588941	0.88[ASN][1000 genomes]
rs28613726	0.88[ASN][1000 genomes]
rs28661791	0.88[ASN][1000 genomes]
rs28696054	0.94[ASN][1000 genomes]
rs28744428	0.94[ASN][1000 genomes]
rs28814696	0.88[ASN][1000 genomes]
rs28819970	0.97[ASN][1000 genomes]
rs28830587	0.88[ASN][1000 genomes]
rs28848573	0.88[ASN][1000 genomes]
rs28855206	0.88[ASN][1000 genomes]
rs28859331	0.88[ASN][1000 genomes]
rs28872587	0.88[ASN][1000 genomes]
rs28877976	0.88[ASN][1000 genomes]
rs28880369	0.88[ASN][1000 genomes]
rs28884892	0.87[ASN][1000 genomes]
rs28893243	0.87[ASN][1000 genomes]
rs34003616	0.86[ASN][1000 genomes]
rs34151233	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34365744	0.88[ASN][1000 genomes]
rs35041609	0.82[AMR][1000 genomes]
rs35107776	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35437107	0.86[ASN][1000 genomes]
rs35639548	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35664299	0.88[ASN][1000 genomes]
rs36051778	0.90[ASN][1000 genomes]
rs3863828	0.94[ASN][1000 genomes]
rs4444815	0.97[ASN][1000 genomes]
rs4475134	0.88[ASN][1000 genomes]
rs57420599	0.86[ASN][1000 genomes]
rs59660596	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67441316	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67906834	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6810417	0.97[ASN][1000 genomes]
rs6858079	0.97[ASN][1000 genomes]
rs71602006	0.88[ASN][1000 genomes]
rs73127077	0.88[ASN][1000 genomes]
rs7660710	0.85[ASN][1000 genomes]
rs7661640	0.88[ASN][1000 genomes]
rs7665615	0.94[ASN][1000 genomes]
rs7667563	0.88[ASN][1000 genomes]
rs7674046	0.97[ASN][1000 genomes]
rs7684329	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7688152	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7691370	0.81[ASN][1000 genomes]
rs7693464	0.97[ASN][1000 genomes]
rs7694031	0.88[ASN][1000 genomes]
rs7694226	0.97[ASN][1000 genomes]
rs9990714	0.86[ASN][1000 genomes]
rs9992483	0.88[ASN][1000 genomes]
rs9993419	0.88[ASN][1000 genomes]
rs9995588	0.88[ASN][1000 genomes]
rs9995797	0.88[ASN][1000 genomes]
rs9997046	0.94[ASN][1000 genomes]

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	nsv1005061	chr4:33366334-33894491	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv878876	chr4:33653757-34000455	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:33818000-33819200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:33818200-33819000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:33818400-33819200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr4:33818400-33819200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr4:33818600-33819200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:33818800-33819200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr4:33818800-33819200	Enhancers	H9 Cell Line	embryonic stem cell
8	chr4:33818800-33819200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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