Variant report

Variant	rs17151318
Chromosome Location	chr8:10060683-10060684
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10085917	0.82[CEU][hapmap]
rs10097315	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10104463	0.81[CEU][hapmap]
rs10283047	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11774836	0.83[CHB][hapmap]
rs11783143	0.80[JPT][hapmap]
rs13257383	0.85[JPT][hapmap]
rs1905630	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs1905631	0.89[CEU][hapmap];0.85[JPT][hapmap]
rs1905633	0.81[AMR][1000 genomes]
rs2409623	0.87[AMR][1000 genomes]
rs28660563	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28701812	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4448276	0.84[CEU][hapmap]
rs57515357	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60032918	0.80[AMR][1000 genomes]
rs62491573	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62491574	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6601420	0.85[CEU][hapmap]
rs6981758	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6982806	0.81[CEU][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6997464	0.85[CEU][hapmap];0.80[JPT][hapmap]
rs7004224	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7006628	0.85[CEU][hapmap];0.85[JPT][hapmap]
rs7011004	0.81[CEU][hapmap]
rs7011281	0.81[CEU][hapmap];0.85[JPT][hapmap]
rs7011821	0.81[CEU][hapmap];0.85[JPT][hapmap]
rs7812517	0.88[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7820236	0.82[CEU][hapmap]
rs7829478	0.89[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7845503	0.89[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	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
4	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
5	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:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10050000-10068000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:10053600-10062400	Weak transcription	Pancreas	Pancrea
3	chr8:10053600-10065000	Weak transcription	Brain Germinal Matrix	brain
4	chr8:10053800-10062400	Weak transcription	Liver	Liver
5	chr8:10053800-10087000	Weak transcription	Spleen	Spleen
6	chr8:10054000-10064200	Weak transcription	Brain Angular Gyrus	brain
7	chr8:10055200-10063800	Weak transcription	Fetal Brain Female	brain
8	chr8:10055400-10074600	Weak transcription	Left Ventricle	heart
9	chr8:10055400-10078400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr8:10055600-10086200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:10056600-10064800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr8:10058400-10062400	Weak transcription	Fetal Brain Male	brain
13	chr8:10058400-10077600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:10058400-10086200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:10058600-10062400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:10059000-10063600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr8:10059200-10061400	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr8:10060000-10060800	ZNF genes & repeats	Lung	lung
19	chr8:10060200-10103000	Weak transcription	Gastric	stomach
20	chr8:10060400-10060800	ZNF genes & repeats	Aorta	Aorta

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