Variant report

Variant	rs9530459
Chromosome Location	chr13:76250576-76250577
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs7322210	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73225927	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7336032	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7338461	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9530458	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9530460	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9530461	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9530462	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9544017	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9544020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9544021	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9544022	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9544023	0.88[AMR][1000 genomes]
rs9544024	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9544025	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9544026	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9565181	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9573612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][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	esv2751152	chr13:76144199-76288418	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv949152	chr13:76211453-76366622	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv900579	chr13:76244056-76307981	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76213400-76267800	Weak transcription	Primary T cells from cord blood	blood
2	chr13:76215400-76258200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:76236800-76267600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr13:76241200-76255600	Weak transcription	HSMMtube	muscle
5	chr13:76244600-76253000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr13:76245200-76251600	Genic enhancers	Osteobl	bone
7	chr13:76247200-76251000	Genic enhancers	HSMM	muscle
8	chr13:76248400-76250800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr13:76248800-76250600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:76248800-76251200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:76249200-76253000	Weak transcription	NH-A	brain
12	chr13:76249400-76253400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr13:76249400-76258800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr13:76249600-76250800	Weak transcription	Aorta	Aorta
15	chr13:76249600-76251600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr13:76249800-76250600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr13:76249800-76250800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr13:76249800-76251000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr13:76249800-76251000	Enhancers	Fetal Lung	lung
20	chr13:76249800-76258800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr13:76250000-76251400	Enhancers	NHLF	lung
22	chr13:76250000-76251600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr13:76250000-76251600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr13:76250000-76258200	Weak transcription	HMEC	breast
25	chr13:76250200-76251000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr13:76250200-76251000	Enhancers	Fetal Stomach	stomach
27	chr13:76250200-76259000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr13:76250200-76262800	Weak transcription	Fetal Brain Male	brain
29	chr13:76250400-76250800	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr13:76250400-76251000	Strong transcription	NHDF-Ad	bronchial
31	chr13:76250400-76251400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr13:76250400-76253000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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