Variant report

Variant	rs10107915
Chromosome Location	chr8:87755123-87755124
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10085929	1.00[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs10109425	0.95[ASN][1000 genomes]
rs10447974	0.83[CEU][hapmap]
rs10504827	0.94[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11774141	0.83[ASN][1000 genomes]
rs11785126	0.94[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12544347	0.82[CEU][hapmap];0.89[CHB][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12549955	0.84[ASN][1000 genomes]
rs1441237	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs1458115	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1458118	0.82[CEU][hapmap]
rs1458130	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1458131	0.83[ASN][1000 genomes]
rs1458133	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16917400	0.94[CEU][hapmap];0.84[CHB][hapmap];0.83[ASN][1000 genomes]
rs16917435	0.84[ASN][1000 genomes]
rs2885471	0.81[JPT][hapmap]
rs4961208	0.82[CEU][hapmap]
rs62525710	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62525739	0.83[ASN][1000 genomes]
rs6990710	0.94[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7460478	0.84[ASN][1000 genomes]
rs7842410	0.81[JPT][hapmap]
rs978132	0.83[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023510	chr8:87429001-87874948	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv891151	chr8:87690019-87776019	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1026794	chr8:87698639-87957840	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv539662	chr8:87698639-87957840	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv817372	chr8:87746712-88292389	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1015760	chr8:87750555-88304604	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87749400-87756000	Weak transcription	Fetal Lung	lung
2	chr8:87754400-87758000	Enhancers	Colon Smooth Muscle	Colon
3	chr8:87754800-87757400	Weak transcription	Fetal Stomach	stomach

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