Variant report

Variant	rs2118739
Chromosome Location	chr15:41493719-41493720
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:41493527..41495439-chr15:41497642..41500215,2	K562	blood:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs12324568	0.86[EUR][1000 genomes]
rs13329240	0.90[ASN][1000 genomes]
rs16952331	0.88[EUR][1000 genomes]
rs16971562	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16971576	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16971647	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16971651	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16971653	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16971654	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16971734	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2083238	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2090826	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2412607	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2412610	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28889391	0.84[ASN][1000 genomes]
rs2899014	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55787465	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55952963	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56262456	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56815966	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57009745	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57896923	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58060180	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58322837	0.90[EUR][1000 genomes]
rs58436082	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58851405	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59441380	0.90[EUR][1000 genomes]
rs59500750	0.84[EUR][1000 genomes]
rs60789744	0.90[EUR][1000 genomes]
rs7165551	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7166182	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7166581	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7167142	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7168706	0.90[EUR][1000 genomes]
rs7172299	0.86[EUR][1000 genomes]
rs7173545	0.84[EUR][1000 genomes]
rs73394302	0.84[EUR][1000 genomes]
rs74012251	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs74012252	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs74012253	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs74012255	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8025660	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8025916	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8026570	0.85[EUR][1000 genomes]
rs8029385	0.90[EUR][1000 genomes]
rs8029694	0.84[EUR][1000 genomes]
rs8030683	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8030706	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8030712	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8030732	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8030954	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8031542	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8038103	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8038575	0.86[EUR][1000 genomes]
rs8039060	0.84[EUR][1000 genomes]
rs8040375	0.90[EUR][1000 genomes]
rs9672272	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9672309	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9745300	0.86[EUR][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	nsv457120	chr15:41410705-41546631	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv569231	chr15:41410705-41546631	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv1039906	chr15:41476209-41518976	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41484400-41494400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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