Variant report

Variant	rs6944237
Chromosome Location	chr7:147154646-147154647
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 107 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:106)

rs_ID	r²[population]
rs1018996	0.90[CEU][hapmap]
rs10242076	0.85[JPT][hapmap]
rs10251234	0.90[CEU][hapmap]
rs10260316	0.90[CEU][hapmap]
rs10260458	0.88[CEU][hapmap]
rs10270551	0.88[CEU][hapmap]
rs10276608	0.88[CEU][hapmap]
rs10281236	0.88[CHB][hapmap];0.85[JPT][hapmap]
rs10282026	0.90[CEU][hapmap]
rs10282126	0.90[CEU][hapmap]
rs10952681	0.90[CEU][hapmap]
rs10952682	0.88[CEU][hapmap]
rs10952683	0.90[CEU][hapmap]
rs10952684	0.90[CEU][hapmap]
rs10952685	0.88[CEU][hapmap]
rs11972784	0.94[CEU][hapmap];0.85[YRI][hapmap]
rs12540164	0.90[CEU][hapmap]
rs12703912	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs12703913	0.88[CEU][hapmap]
rs12703914	0.90[CEU][hapmap]
rs1358540	0.90[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap]
rs1406285	0.85[CEU][hapmap]
rs1468370	0.85[CEU][hapmap]
rs1479846	0.94[CHB][hapmap];0.92[JPT][hapmap]
rs1525220	0.94[CHB][hapmap];0.92[JPT][hapmap]
rs1528515	0.93[CEU][hapmap];0.85[CHB][hapmap];0.92[JPT][hapmap]
rs1528522	0.85[CEU][hapmap]
rs1528527	0.90[CEU][hapmap]
rs1528528	0.90[CEU][hapmap]
rs1528531	0.90[CEU][hapmap]
rs2021879	0.94[CEU][hapmap]
rs2021880	0.90[CEU][hapmap]
rs2022225	0.88[CEU][hapmap];0.85[YRI][hapmap]
rs2178212	0.95[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap]
rs2373132	0.88[CEU][hapmap]
rs2373133	0.88[CEU][hapmap]
rs2373138	0.90[CEU][hapmap]
rs2373139	0.90[CEU][hapmap]
rs2620484	0.95[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap]
rs2620485	0.88[CHB][hapmap];0.92[JPT][hapmap]
rs2888503	0.90[CEU][hapmap];0.82[CHB][hapmap]
rs2888504	0.90[CEU][hapmap]
rs3915305	0.88[CEU][hapmap]
rs4259337	0.90[CEU][hapmap]
rs4725723	0.90[CEU][hapmap]
rs4725725	0.84[CEU][hapmap]
rs4725726	0.90[CEU][hapmap]
rs4725731	0.88[CEU][hapmap]
rs4725732	0.88[CEU][hapmap]
rs4725735	0.90[CEU][hapmap]
rs4725737	0.85[CEU][hapmap]
rs4726860	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs4726861	0.94[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap];0.85[YRI][hapmap]
rs4726864	0.90[CEU][hapmap]
rs4726870	0.83[CEU][hapmap]
rs4726871	0.95[CEU][hapmap]
rs4726872	0.90[CEU][hapmap]
rs6464803	0.95[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap]
rs6464804	0.95[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap]
rs6464805	0.81[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs6464809	0.90[CEU][hapmap]
rs6464810	0.88[CEU][hapmap]
rs6464811	0.90[CEU][hapmap]
rs6464812	0.90[CEU][hapmap]
rs6464813	0.90[CEU][hapmap]
rs6947428	0.88[CEU][hapmap]
rs6972045	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs700294	0.93[CHB][hapmap];0.91[JPT][hapmap]
rs700295	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs700304	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs700305	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs700309	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs7781124	0.95[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs7782093	0.89[CEU][hapmap]
rs7783425	0.88[CEU][hapmap]
rs7783548	0.88[CEU][hapmap]
rs7789396	0.83[CEU][hapmap]
rs7794824	0.90[CEU][hapmap]
rs7796036	0.90[CEU][hapmap]
rs7805836	0.90[CEU][hapmap]
rs7807007	0.95[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap]
rs826643	0.95[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap]
rs826644	1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap]
rs826654	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs826794	0.94[CHB][hapmap];0.92[JPT][hapmap]
rs826795	0.94[CHB][hapmap];0.92[JPT][hapmap]
rs826796	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs826798	0.94[CHB][hapmap];0.92[JPT][hapmap]
rs826799	0.94[CHB][hapmap];0.92[JPT][hapmap]
rs826809	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs826810	0.85[JPT][hapmap]
rs826811	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs826815	0.85[JPT][hapmap]
rs826816	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs826820	0.94[CHB][hapmap];0.92[JPT][hapmap]
rs826821	0.88[CHB][hapmap];0.92[JPT][hapmap]
rs826822	0.85[JPT][hapmap]
rs826824	0.85[JPT][hapmap]
rs826825	0.85[JPT][hapmap]
rs826827	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs826829	0.85[JPT][hapmap]
rs826831	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs861160	0.87[CHB][hapmap];0.92[JPT][hapmap]
rs917125	0.90[CEU][hapmap]
rs917126	0.90[CEU][hapmap]
rs9640243	0.82[CHB][hapmap];0.85[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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