Variant report

Variant	rs7131969
Chromosome Location	chr12:51304856-51304857
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10160844	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10459237	0.81[ASN][1000 genomes]
rs10747597	0.81[ASN][1000 genomes]
rs10747599	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10783393	0.80[ASN][1000 genomes]
rs10783394	0.81[ASN][1000 genomes]
rs10783395	0.87[AMR][1000 genomes]
rs10783404	0.85[ASN][1000 genomes]
rs10783406	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10876099	0.81[ASN][1000 genomes]
rs10876100	0.81[ASN][1000 genomes]
rs10876105	0.82[ASN][1000 genomes]
rs10876115	0.86[ASN][1000 genomes]
rs10876119	0.85[ASN][1000 genomes]
rs1096030	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1096031	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1103441	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11169588	0.81[ASN][1000 genomes]
rs11169589	0.81[ASN][1000 genomes]
rs11169592	0.81[ASN][1000 genomes]
rs11169602	0.86[ASN][1000 genomes]
rs11169603	0.88[ASN][1000 genomes]
rs11169608	0.86[ASN][1000 genomes]
rs11169609	0.86[ASN][1000 genomes]
rs11169610	0.86[ASN][1000 genomes]
rs11169612	0.86[ASN][1000 genomes]
rs11495280	0.83[ASN][1000 genomes]
rs11533636	0.85[ASN][1000 genomes]
rs12578465	0.85[ASN][1000 genomes]
rs12578466	0.85[ASN][1000 genomes]
rs12581103	0.81[ASN][1000 genomes]
rs1362964	0.81[ASN][1000 genomes]
rs1583697	0.81[ASN][1000 genomes]
rs1643004	0.83[ASN][1000 genomes]
rs1659375	0.81[ASN][1000 genomes]
rs2554852	0.83[ASN][1000 genomes]
rs2554854	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3752667	0.84[ASN][1000 genomes]
rs4483656	0.87[ASN][1000 genomes]
rs4768939	0.81[ASN][1000 genomes]
rs73100855	0.80[ASN][1000 genomes]
rs7979616	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs829128	0.82[ASN][1000 genomes]
rs829129	0.82[ASN][1000 genomes]
rs829139	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs829141	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs829142	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs829143	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs829144	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs844175	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs860476	0.81[ASN][1000 genomes]

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	esv3414501	chr12:51174503-51534707	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51303000-51306600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:51304800-51305000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell

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