Variant report

Variant	rs74005915
Chromosome Location	chr15:33930752-33930753
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11630976	0.92[EUR][1000 genomes]
rs11632118	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11634480	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11636955	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11638664	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74005907	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74005909	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74005911	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74005913	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8024924	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs937304	0.94[EUR][1000 genomes]
rs9806579	0.94[EUR][1000 genomes]
rs9806592	0.94[EUR][1000 genomes]

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	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv34037	chr15:33732616-34049083	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33913000-33932200	Weak transcription	Brain Hippocampus Middle	brain
2	chr15:33915000-33959400	Weak transcription	Colon Smooth Muscle	Colon
3	chr15:33920400-33931200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr15:33920800-33931000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr15:33922200-33938400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr15:33923200-33955600	Weak transcription	Brain Cingulate Gyrus	brain
7	chr15:33924200-33932000	Weak transcription	Brain Substantia Nigra	brain
8	chr15:33924400-33931000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr15:33924400-33936400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr15:33925400-33931600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr15:33925800-33952600	Weak transcription	Brain Anterior Caudate	brain
12	chr15:33927800-33931600	Weak transcription	Brain Germinal Matrix	brain
13	chr15:33928400-33931000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:33928800-33931400	Weak transcription	Stomach Smooth Muscle	stomach
15	chr15:33928800-33932000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr15:33928800-33936400	Weak transcription	Aorta	Aorta
17	chr15:33929600-33931400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr15:33930400-33931000	Strong transcription	Fetal Muscle Trunk	muscle
19	chr15:33930400-33931200	Strong transcription	Fetal Muscle Leg	muscle
20	chr15:33930400-33932200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr15:33930400-33932600	Enhancers	Primary B cells from peripheral blood	blood

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