Variant report

Variant	rs68153227
Chromosome Location	chr7:120097017-120097018
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10216253	0.89[ASN][1000 genomes]
rs10225134	0.89[ASN][1000 genomes]
rs10232879	0.91[ASN][1000 genomes]
rs10236303	0.88[ASN][1000 genomes]
rs10241131	0.89[ASN][1000 genomes]
rs10244854	0.93[ASN][1000 genomes]
rs10265776	0.93[ASN][1000 genomes]
rs1029976	0.93[ASN][1000 genomes]
rs10488291	0.89[ASN][1000 genomes]
rs10488292	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10808192	0.93[ASN][1000 genomes]
rs10953913	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10953914	0.93[ASN][1000 genomes]
rs10953915	0.93[ASN][1000 genomes]
rs10953916	0.93[ASN][1000 genomes]
rs10953917	0.93[ASN][1000 genomes]
rs11761549	0.92[ASN][1000 genomes]
rs11763043	0.93[ASN][1000 genomes]
rs11764191	0.93[ASN][1000 genomes]
rs11765472	0.89[ASN][1000 genomes]
rs11767599	0.93[ASN][1000 genomes]
rs11769563	0.92[ASN][1000 genomes]
rs11973307	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12531000	0.93[ASN][1000 genomes]
rs12531689	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12538872	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12672579	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12673578	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12674267	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1476862	0.92[ASN][1000 genomes]
rs17142724	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17142737	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17142741	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1861062	0.89[ASN][1000 genomes]
rs2192374	0.92[ASN][1000 genomes]
rs2402530	0.93[ASN][1000 genomes]
rs2402531	0.93[ASN][1000 genomes]
rs28855094	0.93[ASN][1000 genomes]
rs41391947	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4282509	0.92[ASN][1000 genomes]
rs4534083	0.92[ASN][1000 genomes]
rs6466745	0.89[ASN][1000 genomes]
rs6466746	0.93[ASN][1000 genomes]
rs66843006	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66977230	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67159775	0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67430445	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67436527	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67560031	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs68038367	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6943313	0.93[ASN][1000 genomes]
rs6955059	0.93[ASN][1000 genomes]
rs6962488	0.93[ASN][1000 genomes]
rs6965138	0.93[ASN][1000 genomes]
rs6978518	0.93[ASN][1000 genomes]
rs6979386	0.90[ASN][1000 genomes]
rs6980067	0.93[ASN][1000 genomes]
rs72603599	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72603600	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7776942	0.93[ASN][1000 genomes]
rs7793037	0.93[ASN][1000 genomes]
rs7793195	0.93[ASN][1000 genomes]
rs7793879	0.93[ASN][1000 genomes]
rs7793900	0.93[ASN][1000 genomes]
rs7796685	0.92[ASN][1000 genomes]
rs7798870	0.93[ASN][1000 genomes]
rs7805718	0.93[ASN][1000 genomes]
rs7810837	0.89[ASN][1000 genomes]
rs7811775	0.91[ASN][1000 genomes]
rs9942667	0.93[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	nsv516686	chr7:120015843-120223084	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1026821	chr7:120020317-120190437	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120092000-120101200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:120095400-120098000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr7:120095600-120097400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:120096800-120097200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:120096800-120097200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:120096800-120098000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
7	chr7:120097000-120097200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell

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