Variant report

Variant	rs33974095
Chromosome Location	chr12:42896038-42896039
allele	-/TATA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1017623	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1017624	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1624378	0.81[EUR][1000 genomes]
rs1669931	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1669939	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1669940	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17091311	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1796342	0.81[EUR][1000 genomes]
rs1796344	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1796347	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1796350	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1796369	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1796370	0.82[EUR][1000 genomes]
rs1796371	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2034615	0.82[ASN][1000 genomes]
rs2600906	0.82[ASN][1000 genomes]
rs2600907	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2600925	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2600927	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2600938	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2600939	0.82[ASN][1000 genomes]
rs2708037	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2708038	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2708039	0.82[ASN][1000 genomes]
rs2708040	0.82[ASN][1000 genomes]
rs2708041	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2708042	0.82[ASN][1000 genomes]
rs2708043	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2708044	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2708065	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2708066	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2708067	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34364687	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34817337	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34929717	0.82[ASN][1000 genomes]
rs35541104	0.82[ASN][1000 genomes]
rs67241766	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73128446	0.82[ASN][1000 genomes]
rs73130443	0.82[ASN][1000 genomes]
rs73130454	0.82[ASN][1000 genomes]
rs921530	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs935894	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044790	chr12:42672255-43344184	Enhancers Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
2	nsv541483	chr12:42672255-43344184	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
3	nsv832388	chr12:42878328-43087069	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42878600-42904800	Weak transcription	Right Atrium	heart
2	chr12:42878800-42896400	Weak transcription	Fetal Kidney	kidney
3	chr12:42878800-42898000	Weak transcription	HSMMtube	muscle
4	chr12:42878800-42902000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:42879000-42898000	Weak transcription	NH-A	brain
6	chr12:42879000-42901000	Weak transcription	HSMM	muscle
7	chr12:42884200-42896200	Weak transcription	Lung	lung
8	chr12:42885400-42913600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:42886800-42904800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:42889400-42898000	Weak transcription	Fetal Stomach	stomach
11	chr12:42889800-42902800	Weak transcription	Fetal Muscle Trunk	muscle
12	chr12:42890000-42898600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr12:42890600-42905800	Weak transcription	Osteobl	bone
14	chr12:42891000-42897800	Weak transcription	Fetal Lung	lung
15	chr12:42891000-42898000	Weak transcription	Fetal Muscle Leg	muscle
16	chr12:42891000-42898200	Weak transcription	HUVEC	blood vessel
17	chr12:42891000-42910200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr12:42893000-42896800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:42893000-42901800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:42895200-42896400	Weak transcription	Fetal Heart	heart

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