Variant report

Variant	rs11625869
Chromosome Location	chr14:56315701-56315702
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10134507	0.82[EUR][1000 genomes]
rs11620875	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11621835	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11622627	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11622641	0.83[EUR][1000 genomes]
rs11622710	0.82[EUR][1000 genomes]
rs11624167	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11624516	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11625571	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11626057	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11627629	0.84[EUR][1000 genomes]
rs11628040	0.83[EUR][1000 genomes]
rs12890121	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12894971	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17253841	0.83[EUR][1000 genomes]
rs17832467	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1999705	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1999706	0.85[EUR][1000 genomes]
rs2105058	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2152287	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2342594	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2342595	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28490128	0.88[ASN][1000 genomes]
rs34096981	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34186256	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34421003	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34535564	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34540577	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34663121	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35094937	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs35290945	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35527253	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35559254	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35813917	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs36096896	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36112734	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs36120082	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs36149160	0.84[EUR][1000 genomes]
rs36188950	0.85[EUR][1000 genomes]
rs4601950	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55788205	0.82[EUR][1000 genomes]
rs55837858	0.82[EUR][1000 genomes]
rs57658601	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61975563	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61975579	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61977780	0.83[EUR][1000 genomes]
rs61977781	0.83[EUR][1000 genomes]
rs61977782	0.83[EUR][1000 genomes]
rs61977785	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs71412700	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs999817	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv901966	chr14:56160904-56436203	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv901977	chr14:56213392-56492996	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56311000-56316800	Weak transcription	Stomach Mucosa	stomach
2	chr14:56313400-56316800	Weak transcription	Right Atrium	heart
3	chr14:56313800-56316400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:56314400-56317000	Weak transcription	Adipose Nuclei	Adipose
5	chr14:56314400-56317400	Weak transcription	Hela-S3	cervix
6	chr14:56314600-56317200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr14:56315000-56317000	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr14:56315000-56317400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr14:56315200-56316600	Weak transcription	Aorta	Aorta
10	chr14:56315200-56316800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr14:56315200-56316800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr14:56315200-56317400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:56315200-56317400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr14:56315200-56317400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr14:56315200-56317400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr14:56315200-56317400	Weak transcription	HSMMtube	muscle
17	chr14:56315200-56317400	Weak transcription	NHLF	lung
18	chr14:56315200-56317600	Weak transcription	HSMM	muscle
19	chr14:56315200-56317800	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr14:56315400-56315800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr14:56315400-56317600	Weak transcription	NH-A	brain
22	chr14:56315600-56316800	Weak transcription	NHDF-Ad	bronchial

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