Variant report

Variant	rs11159387
Chromosome Location	chr14:79417235-79417236
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10873319	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs11159385	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11159386	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11159388	1.00[CHB][hapmap];0.94[JPT][hapmap];0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11159389	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11159390	0.95[CHB][hapmap];0.94[JPT][hapmap];0.96[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11845894	0.96[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11847534	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11847702	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12050287	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12588364	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs149088	0.82[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs150774	0.84[JPT][hapmap]
rs154323	0.83[CHB][hapmap];0.89[JPT][hapmap]
rs154329	0.82[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs154330	0.83[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs154333	0.82[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs154334	0.86[ASN][1000 genomes]
rs154336	0.86[ASN][1000 genomes]
rs154340	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs154343	0.87[CHB][hapmap];0.84[JPT][hapmap];0.90[ASN][1000 genomes]
rs154376	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs154378	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs17108397	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs17108401	0.99[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs17108405	0.87[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs17108413	0.99[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs17108429	0.91[CHB][hapmap];0.80[ASN][1000 genomes]
rs220103	0.84[ASN][1000 genomes]
rs220104	0.83[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs2270963	0.91[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs2272292	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2272293	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs31349	0.82[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs31351	0.86[ASN][1000 genomes]
rs31352	0.86[ASN][1000 genomes]
rs31414	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs31415	0.91[CHB][hapmap]
rs31417	0.91[CHB][hapmap]
rs31419	0.80[ASN][1000 genomes]
rs31420	0.91[CHB][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs31421	0.91[CHB][hapmap];0.84[JPT][hapmap]
rs31422	0.91[CHB][hapmap];0.84[JPT][hapmap]
rs31426	0.84[JPT][hapmap]
rs31436	0.88[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs31437	0.87[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs31439	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs31441	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs31448	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs31450	0.83[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs3817535	0.99[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs60746359	0.96[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs61330422	0.96[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs61995265	0.82[ASN][1000 genomes]
rs7142134	1.00[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs7157841	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs730024	0.80[ASN][1000 genomes]
rs8003966	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8007109	0.87[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs8007461	0.87[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs8011529	0.83[CHB][hapmap];0.84[JPT][hapmap]

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	nsv832838	chr14:79306627-79445382	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1048274	chr14:79323592-79417906	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv917249	chr14:79388181-79574717	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041991	chr14:79394408-79644886	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1037112	chr14:79412455-79527656	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79416200-79417800	Enhancers	Fetal Intestine Large	intestine
2	chr14:79416400-79417800	Enhancers	HUVEC	blood vessel
3	chr14:79416600-79417400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr14:79416600-79417400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr14:79416600-79417600	Enhancers	NH-A	brain
6	chr14:79416600-79418000	Enhancers	Fetal Intestine Small	intestine
7	chr14:79416600-79418400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:79416800-79417400	Enhancers	Osteobl	bone
9	chr14:79416800-79418800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:79416800-79426200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr14:79416800-79436000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr14:79417000-79417400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr14:79417000-79417400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr14:79417000-79417400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:79417000-79417400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:79417200-79417400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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