Variant report

Variant	rs2371291
Chromosome Location	chr14:80944887-80944888
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1013010	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10130859	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10146495	0.93[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11159463	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12147045	1.00[ASN][1000 genomes]
rs12587812	0.95[ASN][1000 genomes]
rs12893026	0.80[ASN][1000 genomes]
rs12894863	0.93[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1868631	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1868632	0.87[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2044774	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2122430	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2122433	0.93[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2167149	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2197984	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2197985	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2197987	0.93[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2371292	0.80[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2371293	0.93[ASN][1000 genomes]
rs2371294	0.93[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2371295	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2371297	0.95[ASN][1000 genomes]
rs2371298	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2371299	0.93[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2371300	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2371353	0.93[CEU][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2888003	0.95[ASN][1000 genomes]
rs4627260	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4899770	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4899771	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4899772	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4899773	0.93[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4903916	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4903917	0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4903919	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4903920	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4903921	0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4903922	0.93[CEU][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4903923	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4903924	0.93[CEU][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6574584	0.95[ASN][1000 genomes]
rs7141716	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7143767	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7144280	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7144755	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7156719	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7158378	0.80[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7159700	0.95[ASN][1000 genomes]
rs7160179	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs8003205	0.93[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8016077	0.93[ASN][1000 genomes]
rs8020519	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs935730	0.93[CEU][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:80939200-80980800	Weak transcription	Primary T cells from cord blood	blood
2	chr14:80940400-80949200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:80941000-80945000	Enhancers	NHDF-Ad	bronchial
4	chr14:80941200-80945400	Enhancers	NHLF	lung
5	chr14:80941600-80948800	Weak transcription	Psoas Muscle	Psoas
6	chr14:80941600-80989200	Weak transcription	Left Ventricle	heart
7	chr14:80941800-80956800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr14:80943600-80945000	Enhancers	Dnd41	blood
9	chr14:80944000-80945400	Strong transcription	Skeletal Muscle Female	skeletal muscle
10	chr14:80944200-80949600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr14:80944200-80957600	Weak transcription	Fetal Thymus	thymus
12	chr14:80944600-80956800	Weak transcription	HSMM	muscle

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