Variant report

Variant	rs12056020
Chromosome Location	chr7:147280071-147280072
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10226112	1.00[ASN][1000 genomes]
rs10226376	1.00[ASN][1000 genomes]
rs10226389	1.00[ASN][1000 genomes]
rs10226499	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10227024	0.98[ASN][1000 genomes]
rs10227408	0.86[ASN][1000 genomes]
rs10227633	0.88[ASN][1000 genomes]
rs10229748	0.95[ASN][1000 genomes]
rs10236087	1.00[ASN][1000 genomes]
rs10237202	1.00[ASN][1000 genomes]
rs10240182	1.00[ASN][1000 genomes]
rs10243306	1.00[ASN][1000 genomes]
rs10244825	1.00[ASN][1000 genomes]
rs10245208	1.00[ASN][1000 genomes]
rs10246304	1.00[ASN][1000 genomes]
rs10248888	0.92[ASN][1000 genomes]
rs10250480	1.00[ASN][1000 genomes]
rs10251903	0.92[ASN][1000 genomes]
rs10253397	0.93[ASN][1000 genomes]
rs10255433	1.00[ASN][1000 genomes]
rs10259411	0.89[ASN][1000 genomes]
rs10262765	0.91[ASN][1000 genomes]
rs10269768	0.89[ASN][1000 genomes]
rs10280326	1.00[ASN][1000 genomes]
rs10281966	1.00[ASN][1000 genomes]
rs10952697	1.00[ASN][1000 genomes]
rs1157300	1.00[ASN][1000 genomes]
rs1157301	1.00[ASN][1000 genomes]
rs1157302	1.00[ASN][1000 genomes]
rs12666239	1.00[ASN][1000 genomes]
rs12669822	0.87[ASN][1000 genomes]
rs2051873	0.99[ASN][1000 genomes]
rs2051875	1.00[ASN][1000 genomes]
rs2107858	0.88[ASN][1000 genomes]
rs2107859	0.88[ASN][1000 genomes]
rs2107860	1.00[ASN][1000 genomes]
rs2107861	1.00[ASN][1000 genomes]
rs2158640	1.00[ASN][1000 genomes]
rs2189998	1.00[ASN][1000 genomes]
rs2189999	1.00[ASN][1000 genomes]
rs2373103	1.00[ASN][1000 genomes]
rs2373104	1.00[ASN][1000 genomes]
rs28654757	0.99[ASN][1000 genomes]
rs41354149	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5003022	0.83[ASN][1000 genomes]
rs5003023	0.81[ASN][1000 genomes]
rs5003024	0.99[ASN][1000 genomes]
rs5006631	0.81[ASN][1000 genomes]
rs6464826	1.00[ASN][1000 genomes]
rs6464827	1.00[ASN][1000 genomes]
rs6464828	1.00[ASN][1000 genomes]
rs6464829	1.00[ASN][1000 genomes]
rs6464830	0.89[ASN][1000 genomes]
rs6464831	0.84[ASN][1000 genomes]
rs6943922	0.99[ASN][1000 genomes]
rs6943947	0.82[ASN][1000 genomes]
rs6947921	0.99[ASN][1000 genomes]
rs6947944	0.99[ASN][1000 genomes]
rs6949493	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6954225	0.93[ASN][1000 genomes]
rs6959784	0.89[ASN][1000 genomes]
rs6963584	0.94[ASN][1000 genomes]
rs6967042	0.93[ASN][1000 genomes]
rs6967525	0.94[ASN][1000 genomes]
rs6967857	0.93[ASN][1000 genomes]
rs6973502	1.00[ASN][1000 genomes]
rs6975276	1.00[ASN][1000 genomes]
rs727640	1.00[ASN][1000 genomes]
rs727641	0.98[ASN][1000 genomes]
rs7459220	1.00[ASN][1000 genomes]
rs7780313	1.00[ASN][1000 genomes]
rs7780913	0.87[ASN][1000 genomes]
rs7781205	0.87[ASN][1000 genomes]
rs7781408	0.89[ASN][1000 genomes]
rs7781600	0.88[ASN][1000 genomes]
rs7783132	0.89[ASN][1000 genomes]
rs7796991	0.89[ASN][1000 genomes]
rs7797645	0.89[ASN][1000 genomes]
rs7797918	0.89[ASN][1000 genomes]
rs7799324	0.89[ASN][1000 genomes]
rs7802526	0.89[ASN][1000 genomes]
rs7805454	1.00[ASN][1000 genomes]
rs7805615	1.00[ASN][1000 genomes]
rs7811105	1.00[ASN][1000 genomes]
rs985828	0.83[ASN][1000 genomes]
rs985829	1.00[ASN][1000 genomes]
rs989241	1.00[ASN][1000 genomes]
rs989242	1.00[ASN][1000 genomes]
rs989243	1.00[ASN][1000 genomes]
rs995890	1.00[ASN][1000 genomes]
rs995891	1.00[ASN][1000 genomes]
rs995892	1.00[ASN][1000 genomes]
rs995893	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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
2	esv19066	chr7:147271448-147285044	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv1824789	chr7:147277640-147294703	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv608955	chr7:147279175-147282327	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv608956	chr7:147279175-147283018	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv608957	chr7:147279175-147283342	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv608958	chr7:147279947-147282327	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv608959	chr7:147280000-147283018	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147268000-147283800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:147278400-147283800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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