Variant report

Variant	rs10100022
Chromosome Location	chr8:10052465-10052466
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10087802	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10088890	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10090114	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs10098342	0.90[JPT][hapmap]
rs10216752	0.90[JPT][hapmap]
rs1023961	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs11984513	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs11990555	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs13249486	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs13282106	0.89[JPT][hapmap]
rs1484639	0.89[JPT][hapmap]
rs1484640	0.88[JPT][hapmap]
rs1484642	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs1531918	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs1531919	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs17151071	0.90[JPT][hapmap]
rs17151244	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17689674	0.89[JPT][hapmap]
rs17738724	1.00[CHB][hapmap]
rs17739113	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs17739179	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2046399	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2046400	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2062333	0.88[JPT][hapmap]
rs2220149	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2220150	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2628140	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs28411081	1.00[ASN][1000 genomes]
rs28523656	0.81[AFR][1000 genomes]
rs472514	1.00[CHB][hapmap]
rs4841281	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs4841284	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs58176018	0.85[ASN][1000 genomes]
rs58913892	1.00[ASN][1000 genomes]
rs59337645	0.95[ASN][1000 genomes]
rs60510197	0.95[ASN][1000 genomes]
rs7005350	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs728878	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs73191562	1.00[ASN][1000 genomes]
rs73664934	0.85[ASN][1000 genomes]
rs7812741	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs7823314	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7823557	0.90[ASN][1000 genomes]
rs7823714	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7827921	0.90[ASN][1000 genomes]
rs7832670	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7833387	0.89[JPT][hapmap]
rs7833895	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs7843443	0.84[JPT][hapmap]
rs814405	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs923046	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs9329213	0.90[JPT][hapmap]
rs9329216	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs963592	1.00[CHB][hapmap];0.89[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv610263	chr8:9941021-10090149	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv831230	chr8:9953343-10139350	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1027280	chr8:9958259-10058984	Enhancers Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1021921	chr8:9958259-10212555	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv890344	chr8:9995515-10060638	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv831231	chr8:10001214-10189094	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1026335	chr8:10037279-10139782	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10050000-10057800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:10050000-10068000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:10050200-10053600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr8:10050400-10054600	Weak transcription	HMEC	breast
5	chr8:10050400-10054600	Weak transcription	NHEK	skin
6	chr8:10050400-10055000	Weak transcription	HSMMtube	muscle
7	chr8:10050400-10058000	Weak transcription	Aorta	Aorta
8	chr8:10050600-10054800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr8:10050600-10055000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:10050800-10053800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:10051600-10058400	Enhancers	Fetal Brain Male	brain
12	chr8:10052200-10053600	Enhancers	Fetal Brain Female	brain
13	chr8:10052200-10053800	Enhancers	Liver	Liver
14	chr8:10052200-10054000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr8:10052200-10056200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr8:10052400-10058000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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