Variant report

Variant	rs9589157
Chromosome Location	chr13:91888049-91888050
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:91883445..91885911-chr13:91887432..91889535,2	K562	blood:
2	chr13:91886892..91888652-chr13:91999865..92002715,2	K562	blood:
3	chr13:91885980..91888438-chr13:92037268..92039780,2	K562	blood:
4	chr13:91887562..91890351-chr13:91903749..91905859,2	K562	blood:
5	chr13:91885989..91888652-chr13:91999918..92002715,2	K562	blood:
6	chr13:91886377..91888586-chr13:91890931..91893084,2	K562	blood:
7	chr13:91887222..91888929-chr13:92006604..92009404,2	K562	blood:
8	chr13:91887329..91890707-chr13:91908939..91913306,4	K562	blood:
9	chr13:91886706..91888504-chr13:92053681..92056261,2	K562	blood:
10	chr13:91887562..91890351-chr13:91903749..91906128,3	K562	blood:
11	chr13:91887387..91891925-chr13:91893469..91896614,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000215417	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10454517	1.00[JPT][hapmap]
rs1332221	1.00[JPT][hapmap]
rs16945595	1.00[JPT][hapmap]
rs16945657	1.00[ASN][1000 genomes]
rs16945760	1.00[JPT][hapmap]
rs2026985	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7318410	1.00[JPT][hapmap]
rs7336155	1.00[JPT][hapmap]
rs7358927	1.00[ASN][1000 genomes]
rs7358948	1.00[ASN][1000 genomes]
rs7358999	1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7989029	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7989392	1.00[JPT][hapmap]
rs9301712	1.00[ASN][1000 genomes]
rs9301716	1.00[ASN][1000 genomes]
rs9301723	1.00[JPT][hapmap]
rs9583894	1.00[ASN][1000 genomes]
rs9583899	1.00[ASN][1000 genomes]
rs9583903	1.00[ASN][1000 genomes]
rs9583904	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9589133	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9589136	1.00[ASN][1000 genomes]
rs9589140	1.00[ASN][1000 genomes]
rs9589141	1.00[ASN][1000 genomes]
rs9589142	1.00[ASN][1000 genomes]
rs9589149	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9589150	1.00[JPT][hapmap]
rs9589151	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9589154	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9589155	1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9589156	1.00[ASN][1000 genomes]
rs9589159	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9589161	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9589162	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9589164	1.00[ASN][1000 genomes]
rs9589173	1.00[JPT][hapmap]
rs987770	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	nsv832678	chr13:91771619-91932241	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv2756325	chr13:91836410-91890606	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv2756433	chr13:91841599-91968099	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv832679	chr13:91859467-92030220	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1943 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	chr13:91874600-91890600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr13:91886800-91888400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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