Variant report

Variant	rs9523257
Chromosome Location	chr13:91771522-91771523
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:91771133..91774822-chr13:91777185..91779688,3	K562	blood:

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs1020800	0.90[ASN][1000 genomes]
rs1020801	0.90[ASN][1000 genomes]
rs1174782	0.87[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs1174784	0.87[ASN][1000 genomes]
rs167003	0.89[ASN][1000 genomes]
rs16952571	0.89[ASN][1000 genomes]
rs287490	0.86[ASN][1000 genomes]
rs287491	0.89[ASN][1000 genomes]
rs287494	0.82[ASN][1000 genomes]
rs287495	0.82[ASN][1000 genomes]
rs287497	0.89[ASN][1000 genomes]
rs287498	0.89[ASN][1000 genomes]
rs287501	0.89[ASN][1000 genomes]
rs287505	0.89[ASN][1000 genomes]
rs287506	0.89[ASN][1000 genomes]
rs287509	0.89[ASN][1000 genomes]
rs287510	0.89[ASN][1000 genomes]
rs287511	0.89[ASN][1000 genomes]
rs287512	0.89[ASN][1000 genomes]
rs287513	0.89[ASN][1000 genomes]
rs287514	0.81[ASN][1000 genomes]
rs287515	0.89[ASN][1000 genomes]
rs287517	0.89[ASN][1000 genomes]
rs287518	0.89[ASN][1000 genomes]
rs287519	0.81[JPT][hapmap]
rs287520	0.82[JPT][hapmap]
rs287522	0.89[ASN][1000 genomes]
rs287523	0.88[ASN][1000 genomes]
rs287525	0.89[ASN][1000 genomes]
rs287526	0.89[ASN][1000 genomes]
rs287527	0.80[ASN][1000 genomes]
rs287528	0.90[ASN][1000 genomes]
rs287529	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs287541	0.81[JPT][hapmap]
rs287544	0.81[JPT][hapmap]
rs3764129	0.82[ASN][1000 genomes]
rs476066	0.94[ASN][1000 genomes]
rs492117	0.87[ASN][1000 genomes]
rs502674	0.87[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs505160	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs506173	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs506238	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs512524	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs515029	0.87[ASN][1000 genomes]
rs515097	0.87[ASN][1000 genomes]
rs515850	0.87[ASN][1000 genomes]
rs521178	0.97[ASN][1000 genomes]
rs539504	0.87[ASN][1000 genomes]
rs544464	0.90[ASN][1000 genomes]
rs550731	0.97[ASN][1000 genomes]
rs568455	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs571202	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs582256	0.90[ASN][1000 genomes]
rs583053	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs60671915	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs612195	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs613553	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs620620	0.87[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs623637	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs644953	0.87[ASN][1000 genomes]
rs647785	0.87[ASN][1000 genomes]
rs650892	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs657464	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs665530	0.87[ASN][1000 genomes]
rs684050	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs693016	0.97[ASN][1000 genomes]
rs693721	0.92[ASN][1000 genomes]
rs922083	0.87[ASN][1000 genomes]
rs9515887	0.89[ASN][1000 genomes]
rs9515888	0.89[AMR][1000 genomes]
rs9523263	0.90[ASN][1000 genomes]
rs9523266	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs9560762	0.91[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932206	chr13:91370888-91878374	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1042947	chr13:91571040-92416897	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
3	nsv541871	chr13:91571040-92416897	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
4	nsv900880	chr13:91625722-91848290	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv1803618	chr13:91669587-92277699	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1945 gene(s)	inside rSNPs	diseases
6	nsv900881	chr13:91704312-91829940	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1050259	chr13:91759549-92152078	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1944 gene(s)	inside rSNPs	diseases
8	nsv541872	chr13:91759549-92152078	Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1944 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	chr13:91770600-91772800	Enhancers	GM12878-XiMat	blood

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