Variant report

Variant	rs36093094
Chromosome Location	chr12:29735330-29735331
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs12312423	1.00[EUR][1000 genomes]
rs12422557	1.00[EUR][1000 genomes]
rs12423770	1.00[EUR][1000 genomes]
rs12423941	1.00[EUR][1000 genomes]
rs12424383	1.00[EUR][1000 genomes]
rs12424502	1.00[EUR][1000 genomes]
rs12425004	1.00[EUR][1000 genomes]
rs12426386	1.00[EUR][1000 genomes]
rs12810686	1.00[EUR][1000 genomes]
rs12813081	1.00[EUR][1000 genomes]
rs12817852	1.00[EUR][1000 genomes]
rs12820766	1.00[EUR][1000 genomes]
rs12820809	1.00[EUR][1000 genomes]
rs12822845	1.00[EUR][1000 genomes]
rs12824107	1.00[EUR][1000 genomes]
rs12824420	1.00[EUR][1000 genomes]
rs12826187	1.00[EUR][1000 genomes]
rs12826210	1.00[EUR][1000 genomes]
rs12826354	1.00[EUR][1000 genomes]
rs12826633	1.00[EUR][1000 genomes]
rs12828726	1.00[EUR][1000 genomes]
rs12829843	1.00[EUR][1000 genomes]
rs12831066	1.00[EUR][1000 genomes]
rs28862044	1.00[EUR][1000 genomes]
rs34051575	1.00[EUR][1000 genomes]
rs34211411	1.00[EUR][1000 genomes]
rs34265395	1.00[EUR][1000 genomes]
rs34310782	1.00[EUR][1000 genomes]
rs34377769	1.00[EUR][1000 genomes]
rs34401020	1.00[EUR][1000 genomes]
rs34564434	1.00[EUR][1000 genomes]
rs34598140	1.00[EUR][1000 genomes]
rs34689118	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34769239	1.00[EUR][1000 genomes]
rs34769930	1.00[EUR][1000 genomes]
rs34818263	1.00[EUR][1000 genomes]
rs34867963	1.00[EUR][1000 genomes]
rs34906400	1.00[EUR][1000 genomes]
rs35047658	1.00[EUR][1000 genomes]
rs35205102	1.00[EUR][1000 genomes]
rs35343129	1.00[EUR][1000 genomes]
rs35372963	1.00[EUR][1000 genomes]
rs35425592	1.00[EUR][1000 genomes]
rs35439792	1.00[EUR][1000 genomes]
rs35477340	1.00[EUR][1000 genomes]
rs35666547	1.00[EUR][1000 genomes]
rs35725284	1.00[EUR][1000 genomes]
rs35856698	1.00[EUR][1000 genomes]
rs35957198	1.00[EUR][1000 genomes]
rs36043605	1.00[EUR][1000 genomes]
rs36070392	1.00[EUR][1000 genomes]
rs3825242	1.00[EUR][1000 genomes]
rs7134105	1.00[EUR][1000 genomes]
rs71453743	1.00[EUR][1000 genomes]
rs71453744	1.00[EUR][1000 genomes]
rs71453746	1.00[EUR][1000 genomes]
rs71453747	1.00[EUR][1000 genomes]
rs71453748	1.00[EUR][1000 genomes]
rs71453749	1.00[EUR][1000 genomes]
rs7316470	1.00[EUR][1000 genomes]

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:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29709800-29756200	Weak transcription	HMEC	breast
2	chr12:29713200-29742600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:29716200-29764800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr12:29717600-29736400	Weak transcription	Psoas Muscle	Psoas
5	chr12:29720200-29735800	Weak transcription	Fetal Muscle Trunk	muscle
6	chr12:29720200-29743600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr12:29722400-29735400	Weak transcription	HSMMtube	muscle
8	chr12:29722600-29736400	Weak transcription	Fetal Stomach	stomach
9	chr12:29722800-29735400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:29722800-29735800	Weak transcription	Fetal Kidney	kidney
11	chr12:29725600-29735600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr12:29726000-29751400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:29727800-29735400	Weak transcription	Fetal Heart	heart
14	chr12:29729400-29744000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:29730400-29736200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:29730600-29735600	Weak transcription	Right Ventricle	heart
17	chr12:29731000-29742600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:29731400-29735600	Weak transcription	Small Intestine	intestine
19	chr12:29731800-29769600	Weak transcription	Hela-S3	cervix
20	chr12:29732000-29737200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr12:29732200-29735400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr12:29732200-29737200	Enhancers	Colon Smooth Muscle	Colon
23	chr12:29733600-29736000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr12:29733600-29737000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:29733800-29735800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:29733800-29737200	Enhancers	Adipose Nuclei	Adipose
27	chr12:29734000-29735600	Enhancers	Stomach Smooth Muscle	stomach
28	chr12:29734000-29736600	Enhancers	Brain Anterior Caudate	brain
29	chr12:29734200-29737200	Enhancers	Rectal Smooth Muscle	rectum
30	chr12:29734400-29735400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:29734400-29736200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:29734600-29735800	Enhancers	Liver	Liver
33	chr12:29734600-29737000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr12:29734600-29737000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr12:29734600-29737200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr12:29734800-29735600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr12:29734800-29735800	Enhancers	NH-A	brain
38	chr12:29734800-29736000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
39	chr12:29734800-29736200	Enhancers	Brain Substantia Nigra	brain
40	chr12:29734800-29736800	Enhancers	NHLF	lung
41	chr12:29734800-29737200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr12:29735000-29735400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:29735000-29735600	Enhancers	Osteobl	bone
44	chr12:29735000-29735800	Enhancers	NHDF-Ad	bronchial
45	chr12:29735000-29736000	Enhancers	HUVEC	blood vessel
46	chr12:29735000-29736200	Enhancers	Ovary	ovary
47	chr12:29735200-29735400	Enhancers	Lung	lung
48	chr12:29735200-29735400	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr12:29735200-29735600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr12:29735200-29735600	Enhancers	Duodenum Smooth Muscle	Duodenum

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