Variant report

Variant	rs7863403
Chromosome Location	chr9:73421171-73421172
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1157297	1.00[CHB][hapmap];0.91[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11999610	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12002192	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12002234	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12003052	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12551455	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12552572	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12552632	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12553375	1.00[JPT][hapmap]
rs12554826	0.85[ASN][1000 genomes]
rs12555280	0.86[ASN][1000 genomes]
rs13287453	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1410372	0.83[ASN][1000 genomes]
rs1415232	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs17055861	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34155626	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34322547	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34704982	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35519173	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41315641	0.83[ASN][1000 genomes]
rs55660258	0.85[ASN][1000 genomes]
rs55799488	0.85[ASN][1000 genomes]
rs55905211	0.85[ASN][1000 genomes]
rs56887849	0.85[ASN][1000 genomes]
rs57391768	0.83[ASN][1000 genomes]
rs57760439	0.85[ASN][1000 genomes]
rs57886757	0.85[ASN][1000 genomes]
rs60455022	0.85[ASN][1000 genomes]
rs61256654	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6560154	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7019503	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7020795	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7022747	0.85[ASN][1000 genomes]
rs7024138	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs718447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7861254	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7861859	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7867238	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7868854	0.85[ASN][1000 genomes]
rs7869404	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7870595	0.86[ASN][1000 genomes]
rs7871227	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7872801	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7873058	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7873697	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs913443	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs995902	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs995903	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893440	chr9:73225802-73434585	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	76 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73407400-73427000	Weak transcription	Aorta	Aorta
2	chr9:73411200-73437400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr9:73411800-73433400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:73418200-73444000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:73418200-73447400	Weak transcription	Fetal Kidney	kidney
6	chr9:73420600-73421200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:73420800-73421200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr9:73420800-73421200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr9:73420800-73421200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:73420800-73421200	Enhancers	Adipose Nuclei	Adipose
11	chr9:73420800-73421200	Enhancers	Psoas Muscle	Psoas
12	chr9:73420800-73421200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr9:73420800-73421400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr9:73420800-73421400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:73420800-73421400	Enhancers	Fetal Brain Male	brain
16	chr9:73420800-73421400	Enhancers	Fetal Muscle Leg	muscle
17	chr9:73420800-73421600	Enhancers	Fetal Muscle Trunk	muscle
18	chr9:73421000-73421200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:73421000-73421200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr9:73421000-73421400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:73421000-73421400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:73421000-73421400	Enhancers	Ovary	ovary

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