Variant report

Variant	rs12826911
Chromosome Location	chr12:29719666-29719667
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:29713988..29716071-chr12:29717724..29720269,2	K562	blood:

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs11829731	0.89[CHB][hapmap]
rs11834291	0.89[CHB][hapmap]
rs12422557	0.94[AMR][1000 genomes]
rs12423770	1.00[AMR][1000 genomes]
rs12423941	1.00[AMR][1000 genomes]
rs12424383	0.88[AMR][1000 genomes]
rs12425004	1.00[AMR][1000 genomes]
rs12426386	1.00[AMR][1000 genomes]
rs12810686	1.00[AMR][1000 genomes]
rs12813081	1.00[AMR][1000 genomes]
rs12817852	1.00[AMR][1000 genomes]
rs12820809	1.00[AMR][1000 genomes]
rs12822100	1.00[CHB][hapmap]
rs12822845	0.88[AMR][1000 genomes]
rs12824107	1.00[AMR][1000 genomes]
rs12824420	1.00[AMR][1000 genomes]
rs12826187	1.00[AMR][1000 genomes]
rs12826210	1.00[AMR][1000 genomes]
rs12826893	1.00[CHB][hapmap]
rs12828726	1.00[AMR][1000 genomes]
rs12828728	1.00[CHB][hapmap]
rs12829843	1.00[AMR][1000 genomes]
rs142565	1.00[CHB][hapmap]
rs148897	0.89[CHB][hapmap]
rs159688	1.00[CHB][hapmap]
rs159691	1.00[CHB][hapmap]
rs159692	1.00[CHB][hapmap]
rs16934418	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16934523	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16934537	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16934564	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs16934569	0.89[CHB][hapmap]
rs16934597	0.89[CHB][hapmap]
rs16934635	1.00[CHB][hapmap]
rs28862044	0.88[AMR][1000 genomes]
rs299450	1.00[AMR][1000 genomes]
rs299477	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs299478	1.00[CHB][hapmap]
rs299482	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs299483	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs299485	1.00[CHB][hapmap]
rs34051575	1.00[AMR][1000 genomes]
rs34211411	1.00[AMR][1000 genomes]
rs34265395	1.00[AMR][1000 genomes]
rs34310782	1.00[AMR][1000 genomes]
rs34384320	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34401020	1.00[AMR][1000 genomes]
rs34598140	1.00[AMR][1000 genomes]
rs34818263	1.00[AMR][1000 genomes]
rs34867963	1.00[AMR][1000 genomes]
rs34906400	1.00[AMR][1000 genomes]
rs35047658	1.00[AMR][1000 genomes]
rs35205102	1.00[AMR][1000 genomes]
rs35343129	1.00[AMR][1000 genomes]
rs35372963	1.00[AMR][1000 genomes]
rs35439792	1.00[AMR][1000 genomes]
rs35477340	1.00[AMR][1000 genomes]
rs35666547	1.00[AMR][1000 genomes]
rs35725284	1.00[AMR][1000 genomes]
rs35856698	1.00[AMR][1000 genomes]
rs36043605	1.00[AMR][1000 genomes]
rs36070392	1.00[AMR][1000 genomes]
rs3825242	1.00[AMR][1000 genomes]
rs71453743	1.00[AMR][1000 genomes]
rs71453744	1.00[AMR][1000 genomes]
rs71453746	1.00[AMR][1000 genomes]
rs71453747	0.88[AMR][1000 genomes]
rs7301943	0.89[CHB][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	nsv1053641	chr12:29268813-29854413	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv469190	chr12:29612425-29811471	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv557917	chr12:29612425-29811471	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv1053629	chr12:29680163-29826626	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv529328	chr12:29692414-30246209	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29665400-29725400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr12:29700400-29734000	Weak transcription	Brain Anterior Caudate	brain
3	chr12:29709800-29756200	Weak transcription	HMEC	breast
4	chr12:29711800-29720800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:29712600-29722200	Weak transcription	Colonic Mucosa	Colon
6	chr12:29712600-29734600	Weak transcription	Liver	Liver
7	chr12:29712800-29722200	Weak transcription	Brain Germinal Matrix	brain
8	chr12:29713200-29719800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr12:29713200-29719800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr12:29713200-29726400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr12:29713200-29726600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr12:29713200-29731200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr12:29713200-29742600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:29715400-29721400	Weak transcription	Esophagus	oesophagus
15	chr12:29715400-29722200	Weak transcription	Fetal Lung	lung
16	chr12:29715400-29731200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:29715800-29724800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:29716200-29764800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr12:29716400-29721000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:29716400-29722200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:29717000-29720000	Weak transcription	Right Atrium	heart
22	chr12:29717000-29721800	Weak transcription	HUVEC	blood vessel
23	chr12:29717400-29720400	Weak transcription	Fetal Heart	heart
24	chr12:29717400-29722200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr12:29717600-29721600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr12:29717600-29721600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr12:29717600-29725000	Weak transcription	Aorta	Aorta
28	chr12:29717600-29727400	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr12:29717600-29727800	Weak transcription	Duodenum Mucosa	Duodenum
30	chr12:29717600-29734800	Weak transcription	NHLF	lung
31	chr12:29717600-29736400	Weak transcription	Psoas Muscle	Psoas
32	chr12:29717800-29719800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:29717800-29721600	Weak transcription	HSMMtube	muscle
34	chr12:29717800-29732200	Weak transcription	Colon Smooth Muscle	Colon
35	chr12:29718000-29720000	Weak transcription	Hela-S3	cervix
36	chr12:29718000-29720200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:29718200-29720000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr12:29718200-29725400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr12:29718600-29727600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr12:29718800-29719800	Genic enhancers	Spleen	Spleen
41	chr12:29718800-29720200	Enhancers	Ovary	ovary
42	chr12:29718800-29723000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:29719000-29719800	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr12:29719000-29720000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:29719000-29720000	Genic enhancers	Left Ventricle	heart
46	chr12:29719000-29720000	Enhancers	Lung	lung
47	chr12:29719000-29720000	Bivalent Enhancer	Stomach Mucosa	stomach
48	chr12:29719000-29720200	Enhancers	Gastric	stomach
49	chr12:29719200-29720000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr12:29719200-29720000	Genic enhancers	Muscle Satellite Cultured Cells	--

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