Variant report

Variant	rs4238071
Chromosome Location	chr12:40154281-40154282
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10083196	1.00[CEU][hapmap]
rs10444571	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10444572	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10747879	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10784058	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11829443	0.93[AFR][1000 genomes]
rs11829551	1.00[YRI][hapmap]
rs11829985	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs11830107	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs11830110	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs11830326	1.00[YRI][hapmap]
rs11830355	0.93[AFR][1000 genomes]
rs11831388	0.86[LWK][hapmap];0.84[MKK][hapmap]
rs11833656	1.00[YRI][hapmap]
rs11833798	1.00[CEU][hapmap]
rs11834401	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs11835330	0.93[AFR][1000 genomes]
rs11835385	0.93[AFR][1000 genomes]
rs4238074	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4238075	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4238077	0.82[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4238078	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[EUR][1000 genomes]
rs4267135	0.95[EUR][1000 genomes]
rs4268570	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4321021	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4322462	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4334097	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4334098	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs4334099	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs4374002	1.00[ASN][1000 genomes]
rs4391873	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4397917	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4399379	1.00[CEU][hapmap]
rs4426190	0.94[EUR][1000 genomes]
rs4427625	1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes]
rs4435073	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs4441086	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4447240	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4450227	1.00[ASN][1000 genomes]
rs4511345	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4529945	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4533100	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4544077	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4576894	0.81[EUR][1000 genomes]
rs4583047	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4611277	1.00[ASN][1000 genomes]
rs4639999	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[EUR][1000 genomes]
rs4767953	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4768173	1.00[ASN][1000 genomes]
rs4768175	1.00[ASN][1000 genomes]
rs4768176	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4768178	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4768180	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4768181	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs4768182	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs56122050	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6581321	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6581325	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6581326	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6581336	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6581337	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6581338	1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes]
rs6581346	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7133037	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7135021	1.00[ASN][1000 genomes]
rs7135047	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7297063	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7299595	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7300946	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7302571	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7303581	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7310917	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7956254	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7961216	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7967287	1.00[ASN][1000 genomes]
rs7967347	1.00[ASN][1000 genomes]
rs7969296	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7973782	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7975209	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs9645805	1.00[CEU][hapmap];0.95[EUR][1000 genomes]

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	nsv531527	chr12:39680812-40182822	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1037457	chr12:39898349-40245401	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv541480	chr12:39898349-40245401	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv899024	chr12:40046408-40188870	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1053603	chr12:40082673-40197609	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv427907	chr12:40122713-40199621	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv428280	chr12:40122713-40199621	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40130800-40156400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr12:40143800-40156800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr12:40144200-40156200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:40144200-40157600	Weak transcription	Pancreas	Pancrea
5	chr12:40144800-40166400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:40145000-40175000	Weak transcription	Right Ventricle	heart
7	chr12:40145600-40157400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr12:40146000-40166800	Weak transcription	Ovary	ovary
9	chr12:40146200-40157200	Weak transcription	Aorta	Aorta
10	chr12:40146200-40157200	Weak transcription	Left Ventricle	heart
11	chr12:40146200-40159000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr12:40147400-40157200	Weak transcription	Adipose Nuclei	Adipose
13	chr12:40148000-40157000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:40148200-40157000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr12:40150000-40157200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:40150200-40160400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr12:40151400-40160600	Weak transcription	NHDF-Ad	bronchial
18	chr12:40151600-40157200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:40151800-40160800	Weak transcription	Colon Smooth Muscle	Colon
20	chr12:40152400-40156400	Weak transcription	Stomach Smooth Muscle	stomach
21	chr12:40152800-40159600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr12:40153200-40157200	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr12:40153200-40171400	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr12:40153400-40155800	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr12:40153600-40156000	Weak transcription	Fetal Kidney	kidney
26	chr12:40154000-40155000	Strong transcription	Fetal Intestine Large	intestine
27	chr12:40154200-40154800	Strong transcription	Liver	Liver
28	chr12:40154200-40157600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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