Variant report

Variant	rs67436527
Chromosome Location	chr7:120043258-120043259
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10216253	0.91[ASN][1000 genomes]
rs10225134	0.91[ASN][1000 genomes]
rs10232879	0.90[ASN][1000 genomes]
rs10236303	0.89[ASN][1000 genomes]
rs10241131	0.91[ASN][1000 genomes]
rs10244854	0.87[ASN][1000 genomes]
rs10265776	0.87[ASN][1000 genomes]
rs1029976	0.87[ASN][1000 genomes]
rs10488291	0.91[ASN][1000 genomes]
rs10488292	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10808192	0.87[ASN][1000 genomes]
rs10953913	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10953914	0.87[ASN][1000 genomes]
rs10953915	0.87[ASN][1000 genomes]
rs10953916	0.87[ASN][1000 genomes]
rs10953917	0.87[ASN][1000 genomes]
rs11761549	0.89[ASN][1000 genomes]
rs11763043	0.87[ASN][1000 genomes]
rs11764191	0.87[ASN][1000 genomes]
rs11765472	0.91[ASN][1000 genomes]
rs11767599	0.87[ASN][1000 genomes]
rs11769563	0.89[ASN][1000 genomes]
rs11973307	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12531000	0.87[ASN][1000 genomes]
rs12531689	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12538872	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12672579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12673578	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12674267	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1476862	0.89[ASN][1000 genomes]
rs17142724	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17142737	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17142741	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1861062	0.83[ASN][1000 genomes]
rs2192374	0.86[ASN][1000 genomes]
rs2402530	0.87[ASN][1000 genomes]
rs2402531	0.87[ASN][1000 genomes]
rs28855094	0.87[ASN][1000 genomes]
rs41391947	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4282509	0.89[ASN][1000 genomes]
rs4534083	0.89[ASN][1000 genomes]
rs6466745	0.91[ASN][1000 genomes]
rs6466746	0.87[ASN][1000 genomes]
rs66843006	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66977230	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67159775	0.98[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67430445	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67560031	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs68038367	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs68153227	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6943313	0.87[ASN][1000 genomes]
rs6955059	0.87[ASN][1000 genomes]
rs6962488	0.87[ASN][1000 genomes]
rs6965138	0.87[ASN][1000 genomes]
rs6978518	0.87[ASN][1000 genomes]
rs6979386	0.89[ASN][1000 genomes]
rs6980067	0.87[ASN][1000 genomes]
rs72603599	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72603600	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7776942	0.87[ASN][1000 genomes]
rs7793037	0.87[ASN][1000 genomes]
rs7793195	0.87[ASN][1000 genomes]
rs7793879	0.87[ASN][1000 genomes]
rs7793900	0.87[ASN][1000 genomes]
rs7796685	0.89[ASN][1000 genomes]
rs7798870	0.87[ASN][1000 genomes]
rs7805718	0.87[ASN][1000 genomes]
rs7810837	0.91[ASN][1000 genomes]
rs7811775	0.90[ASN][1000 genomes]
rs9942667	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024920	chr7:120002420-120083753	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	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
3	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:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120041200-120043400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr7:120041600-120044800	Enhancers	NHEK	skin
3	chr7:120041800-120043400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:120041800-120043400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:120042000-120043400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr7:120042000-120044600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:120042200-120043400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr7:120042200-120043400	Enhancers	Rectal Smooth Muscle	rectum
9	chr7:120042200-120043400	Enhancers	NH-A	brain
10	chr7:120042200-120044200	Enhancers	HMEC	breast
11	chr7:120042200-120044800	Enhancers	Hela-S3	cervix
12	chr7:120042600-120043600	Enhancers	HUVEC	blood vessel
13	chr7:120042600-120044800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr7:120042800-120043400	Flanking Active TSS	GM12878-XiMat	blood
15	chr7:120042800-120043800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr7:120043000-120044400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:120043200-120044200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr7:120043200-120044200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr7:120043200-120044200	Weak transcription	Stomach Mucosa	stomach
20	chr7:120043200-120075000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links