Variant report

Variant	rs11182360
Chromosome Location	chr12:44366739-44366740
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11182302	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs11182309	0.81[ASN][1000 genomes]
rs11182362	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182365	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182369	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182373	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182378	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182379	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182381	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11182383	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182384	1.00[CHB][hapmap]
rs11182385	1.00[CHB][hapmap]
rs11182386	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182387	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182388	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182390	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182391	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182394	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182396	1.00[CHB][hapmap]
rs11182399	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182403	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182405	1.00[CHB][hapmap]
rs11182406	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182409	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182413	1.00[AMR][1000 genomes]
rs12099769	1.00[CHB][hapmap]
rs12228693	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12231403	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12231978	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs1565620	1.00[CHB][hapmap]
rs17094057	1.00[AMR][1000 genomes]
rs17094127	1.00[AMR][1000 genomes]
rs17094138	1.00[AMR][1000 genomes]
rs17094142	1.00[AMR][1000 genomes]
rs1976211	1.00[CHB][hapmap]
rs2012087	1.00[AMR][1000 genomes]
rs3858723	1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3929354	1.00[CHB][hapmap]
rs6582494	1.00[JPT][hapmap]
rs6582495	1.00[CHB][hapmap]
rs7959226	1.00[CHB][hapmap]
rs7980005	1.00[CHB][hapmap]
rs8181703	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9919742	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832390	chr12:44318071-44512114	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1041188	chr12:44331098-44528712	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44342000-44367200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr12:44343600-44376800	Weak transcription	Pancreas	Pancrea
3	chr12:44354400-44367000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:44356200-44368000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:44358800-44367800	Weak transcription	Esophagus	oesophagus
6	chr12:44361400-44401400	Weak transcription	Aorta	Aorta
7	chr12:44363800-44382400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:44364600-44369600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:44364600-44370000	Weak transcription	HMEC	breast
10	chr12:44364600-44393200	Weak transcription	Small Intestine	intestine
11	chr12:44364800-44377000	Weak transcription	Left Ventricle	heart
12	chr12:44366000-44375600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:44366200-44373400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:44366400-44367000	Weak transcription	Fetal Intestine Small	intestine
15	chr12:44366600-44367800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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