Variant report

Variant	rs9523996
Chromosome Location	chr13:93934631-93934632
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	chr13:93933342..93934881-chr13:108607842..108609818,2	K562	blood:
2	chr13:93924002..93926974-chr13:93932644..93934899,3	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10507998	0.92[CEU][hapmap];0.83[CHB][hapmap];0.85[YRI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1323997	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[MEX][hapmap]
rs1328373	0.92[CEU][hapmap];1.00[CHB][hapmap]
rs16948616	0.92[CEU][hapmap];0.88[CHB][hapmap];0.80[EUR][1000 genomes]
rs17267544	0.93[CEU][hapmap];0.88[CHB][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17267585	0.91[ASW][hapmap];0.92[CEU][hapmap];0.83[CHB][hapmap];0.89[GIH][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.97[TSI][hapmap];0.85[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2025948	0.85[CEU][hapmap];0.83[CHB][hapmap]
rs2057525	0.92[CEU][hapmap];0.82[MEX][hapmap]
rs4142602	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];0.89[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72635668	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72635674	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9301866	0.92[CEU][hapmap];1.00[CHB][hapmap]
rs9516201	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9516203	0.93[CEU][hapmap];0.89[CHB][hapmap];0.81[GIH][hapmap];0.83[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.92[TSI][hapmap];0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9516204	0.92[CEU][hapmap];0.88[CHB][hapmap];0.83[JPT][hapmap];0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9516205	0.92[CEU][hapmap];0.88[CHB][hapmap];0.83[JPT][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9516208	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9523984	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9523985	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9523992	0.91[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9523993	0.93[CEU][hapmap];0.89[CHB][hapmap];0.95[GIH][hapmap];0.83[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.94[TSI][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9523994	0.91[CEU][hapmap]
rs9523995	0.92[CEU][hapmap];0.89[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9524000	0.83[CHB][hapmap]
rs9524001	0.92[CEU][hapmap];0.89[CHB][hapmap];0.82[GIH][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9561296	0.92[CEU][hapmap];0.89[CHB][hapmap];0.83[JPT][hapmap];0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9561297	0.81[ASW][hapmap];0.93[CEU][hapmap];0.89[CHB][hapmap];0.95[GIH][hapmap];0.83[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.94[TSI][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9561300	0.92[CEU][hapmap];0.89[CHB][hapmap];0.82[GIH][hapmap];0.86[MEX][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9561305	0.92[CEU][hapmap];1.00[CHB][hapmap];0.82[MEX][hapmap]
rs9561306	0.92[CEU][hapmap];1.00[CHB][hapmap]

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	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1053035	chr13:93842576-94229732	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv541880	chr13:93842576-94229732	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2751156	chr13:93912999-93988638	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93923800-93935600	Weak transcription	Ovary	ovary
2	chr13:93924400-93942000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr13:93929000-93953800	Weak transcription	Right Atrium	heart
4	chr13:93932400-93952200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:93932600-93938600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr13:93933000-93938200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr13:93933200-93938400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr13:93933400-93938000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr13:93933400-93938200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr13:93934200-93934800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr13:93934200-93934800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr13:93934400-93934800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr13:93934600-93934800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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