Variant report

Variant	rs10803923
Chromosome Location	chr2:179931060-179931061
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10497530	0.81[AMR][1000 genomes]
rs10497531	0.83[AMR][1000 genomes]
rs10497532	0.83[AMR][1000 genomes]
rs11883598	0.83[AMR][1000 genomes]
rs11883599	0.83[AMR][1000 genomes]
rs11883748	0.83[AMR][1000 genomes]
rs11893153	0.83[AMR][1000 genomes]
rs11899563	0.83[AMR][1000 genomes]
rs11902355	0.81[AMR][1000 genomes]
rs11903793	0.83[AMR][1000 genomes]
rs13009130	0.89[AMR][1000 genomes]
rs13032202	0.89[AMR][1000 genomes]
rs1875779	0.81[AMR][1000 genomes]
rs34190485	0.87[AMR][1000 genomes]
rs35465824	0.83[AMR][1000 genomes]
rs35888089	0.83[AMR][1000 genomes]
rs35901501	0.85[AMR][1000 genomes]
rs35979436	0.81[AMR][1000 genomes]
rs36098953	0.89[AMR][1000 genomes]
rs4991006	0.81[AMR][1000 genomes]
rs62175401	0.83[AMR][1000 genomes]
rs62175403	0.83[AMR][1000 genomes]
rs62175413	0.89[AMR][1000 genomes]
rs62175419	0.87[AMR][1000 genomes]
rs62175420	0.83[AMR][1000 genomes]
rs62175421	0.83[AMR][1000 genomes]
rs62175422	0.83[AMR][1000 genomes]
rs6433747	0.83[AMR][1000 genomes]
rs6433748	0.83[AMR][1000 genomes]
rs6433749	0.83[AMR][1000 genomes]
rs6433750	0.83[AMR][1000 genomes]
rs6433751	0.83[AMR][1000 genomes]
rs6433752	0.83[AMR][1000 genomes]
rs6731564	0.83[AMR][1000 genomes]
rs6731566	0.83[AMR][1000 genomes]
rs6734597	0.81[AMR][1000 genomes]
rs7574853	0.83[AMR][1000 genomes]
rs7575047	0.83[AMR][1000 genomes]
rs7578521	0.81[AMR][1000 genomes]
rs7578961	0.83[AMR][1000 genomes]
rs7579263	0.83[AMR][1000 genomes]
rs7582862	0.83[AMR][1000 genomes]
rs7588765	0.83[AMR][1000 genomes]
rs7596842	0.83[AMR][1000 genomes]
rs7601179	0.83[AMR][1000 genomes]
rs7605060	0.87[AMR][1000 genomes]
rs7609150	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949133	chr2:179711376-180124327	Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv875457	chr2:179775893-179966804	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875458	chr2:179780624-179966804	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv875464	chr2:179843612-179939493	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv875465	chr2:179843612-179966804	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv508184	chr2:179896384-179965419	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179923600-179933800	Weak transcription	Gastric	stomach
2	chr2:179924800-179931600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:179930800-179931200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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