Variant report

Variant	rs12756153
Chromosome Location	chr1:183975659-183975660
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12089543	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12727244	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12741795	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12746606	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12748062	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12753441	0.86[EUR][1000 genomes]
rs12756229	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12758284	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12760593	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34922778	1.00[ASN][1000 genomes]
rs35418511	1.00[ASN][1000 genomes]
rs4650648	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4651163	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs751411	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530079	chr1:183797938-184639971	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv533206	chr1:183861204-184091272	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1006655	chr1:183922288-184186677	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv872583	chr1:183955574-184015663	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:183971600-183977600	Weak transcription	Gastric	stomach
2	chr1:183971600-183978800	Weak transcription	Right Ventricle	heart
3	chr1:183972400-183983000	Weak transcription	NHDF-Ad	bronchial
4	chr1:183972600-183975800	Weak transcription	Left Ventricle	heart
5	chr1:183972600-183976200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:183972600-183980600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:183972600-183987800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:183974200-183977000	Enhancers	Brain Substantia Nigra	brain
9	chr1:183974600-183976000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr1:183974600-183979400	Weak transcription	Brain Hippocampus Middle	brain
11	chr1:183974800-183981600	Weak transcription	Brain Angular Gyrus	brain
12	chr1:183975000-183976200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:183975000-183976200	Weak transcription	Brain Anterior Caudate	brain
14	chr1:183975000-183978600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr1:183975000-183980000	Weak transcription	Fetal Muscle Leg	muscle
16	chr1:183975200-183981600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr1:183975600-183976000	Weak transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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