Variant report

Variant	rs1526518
Chromosome Location	chr7:11809623-11809624
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10239072	0.85[EUR][1000 genomes]
rs10265139	0.93[ASN][1000 genomes]
rs10276715	0.93[ASN][1000 genomes]
rs10499405	0.88[CHD][hapmap];0.92[JPT][hapmap]
rs10950366	0.86[JPT][hapmap]
rs12667493	0.81[CHB][hapmap];0.88[CHD][hapmap];0.86[JPT][hapmap]
rs12667512	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs12671899	0.81[CHB][hapmap];0.88[CHD][hapmap];0.86[JPT][hapmap]
rs12673487	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1465007	0.85[ASN][1000 genomes]
rs1465008	0.85[ASN][1000 genomes]
rs1467344	0.83[ASN][1000 genomes]
rs1467345	0.85[ASN][1000 genomes]
rs1526521	0.85[ASN][1000 genomes]
rs1526555	0.92[ASN][1000 genomes]
rs17165172	0.88[ASN][1000 genomes]
rs17165181	0.90[ASN][1000 genomes]
rs2355077	0.85[ASN][1000 genomes]
rs2355085	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2883592	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4506091	0.81[ASN][1000 genomes]
rs55668447	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55709709	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55786242	0.88[ASN][1000 genomes]
rs55860284	0.90[ASN][1000 genomes]
rs56020952	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57417976	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57623191	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57645050	0.90[ASN][1000 genomes]
rs57822376	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58325377	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58747700	0.87[ASN][1000 genomes]
rs60510202	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62433414	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62435372	0.83[EUR][1000 genomes]
rs6460838	0.83[ASN][1000 genomes]
rs6460839	0.83[ASN][1000 genomes]
rs6460843	0.84[EUR][1000 genomes]
rs66791240	0.90[ASN][1000 genomes]
rs66894282	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs67195807	0.90[ASN][1000 genomes]
rs67255535	0.87[ASN][1000 genomes]
rs67907409	0.93[ASN][1000 genomes]
rs68076870	0.93[ASN][1000 genomes]
rs6957349	0.85[ASN][1000 genomes]
rs6960116	0.81[CHB][hapmap];0.88[CHD][hapmap];0.86[JPT][hapmap]
rs6973826	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs6973931	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs73298449	0.93[ASN][1000 genomes]
rs7788213	0.83[ASN][1000 genomes]
rs7794473	0.83[EUR][1000 genomes]
rs7795628	0.90[ASN][1000 genomes]
rs7802597	0.84[JPT][hapmap]
rs9691520	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs999879	0.85[ASN][1000 genomes]
rs999880	0.85[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	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv830905	chr7:11793513-11941594	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 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	chr7:11800400-11811200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:11809600-11810400	Enhancers	A549	lung

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