Variant report

Variant	rs9515852
Chromosome Location	chr13:91573608-91573609
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:91569478..91571277-chr13:91572138..91574346,2	K562	blood:
2	chr13:91567416..91569348-chr13:91571429..91575596,3	K562	blood:

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10507986	0.84[ASN][1000 genomes]
rs12184671	0.96[ASN][1000 genomes]
rs12866129	0.91[ASN][1000 genomes]
rs12873242	0.92[ASN][1000 genomes]
rs1335553	0.92[ASN][1000 genomes]
rs1335556	0.96[ASN][1000 genomes]
rs1335560	0.92[ASN][1000 genomes]
rs1335563	0.88[EUR][1000 genomes]
rs1335575	0.92[ASN][1000 genomes]
rs1335576	0.92[ASN][1000 genomes]
rs1376746	0.92[ASN][1000 genomes]
rs1376747	0.91[ASN][1000 genomes]
rs1591447	0.84[EUR][1000 genomes]
rs1597701	0.81[ASN][1000 genomes]
rs17667080	0.92[ASN][1000 genomes]
rs17667353	0.92[ASN][1000 genomes]
rs17667370	0.81[ASN][1000 genomes]
rs17667393	0.81[ASN][1000 genomes]
rs17734926	0.81[ASN][1000 genomes]
rs2123011	0.90[ASN][1000 genomes]
rs2860120	0.91[ASN][1000 genomes]
rs34383868	0.96[ASN][1000 genomes]
rs34636886	0.89[ASN][1000 genomes]
rs34874149	0.96[ASN][1000 genomes]
rs35044404	0.96[ASN][1000 genomes]
rs4537875	0.80[ASN][1000 genomes]
rs4624029	0.80[ASN][1000 genomes]
rs4773602	0.91[ASN][1000 genomes]
rs4773603	0.92[ASN][1000 genomes]
rs4773604	0.92[ASN][1000 genomes]
rs55962639	0.96[ASN][1000 genomes]
rs61968264	0.91[ASN][1000 genomes]
rs61968265	0.91[ASN][1000 genomes]
rs61968294	0.90[ASN][1000 genomes]
rs67008524	0.96[ASN][1000 genomes]
rs717457	0.95[ASN][1000 genomes]
rs723346	0.96[ASN][1000 genomes]
rs7350640	0.84[ASN][1000 genomes]
rs747222	0.96[ASN][1000 genomes]
rs9515838	0.84[ASN][1000 genomes]
rs9515841	0.92[ASN][1000 genomes]
rs9515842	0.91[ASN][1000 genomes]
rs9515849	0.96[ASN][1000 genomes]
rs9515850	0.96[ASN][1000 genomes]
rs9515851	0.96[ASN][1000 genomes]
rs9523156	0.84[EUR][1000 genomes]
rs9523158	0.84[ASN][1000 genomes]
rs9523169	0.92[ASN][1000 genomes]
rs9523170	0.91[ASN][1000 genomes]
rs9523171	0.92[ASN][1000 genomes]
rs9523172	0.91[ASN][1000 genomes]
rs9523173	0.92[ASN][1000 genomes]
rs9523177	0.91[ASN][1000 genomes]
rs9523180	0.96[ASN][1000 genomes]
rs9523181	0.96[ASN][1000 genomes]
rs9523182	0.96[ASN][1000 genomes]
rs9523183	0.96[ASN][1000 genomes]
rs9523188	0.96[ASN][1000 genomes]
rs9523190	0.96[ASN][1000 genomes]
rs9523193	0.96[ASN][1000 genomes]
rs9523195	0.95[ASN][1000 genomes]
rs9523196	0.91[ASN][1000 genomes]
rs9523197	0.92[ASN][1000 genomes]
rs9523205	0.81[ASN][1000 genomes]
rs9523209	0.81[ASN][1000 genomes]
rs9523213	0.80[ASN][1000 genomes]
rs9523215	0.80[ASN][1000 genomes]
rs977991	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948709	chr13:90753085-91745571	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:91559600-91581000	Weak transcription	Right Atrium	heart
2	chr13:91572000-91578200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:91573400-91578800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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