Variant report

Variant	rs7148370
Chromosome Location	chr14:38442525-38442526
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10134624	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10140719	1.00[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10145136	1.00[CEU][hapmap]
rs10145337	0.91[EUR][1000 genomes]
rs10146385	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10483495	0.89[CEU][hapmap]
rs10872905	0.96[CEU][hapmap]
rs1113092	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11156973	1.00[CEU][hapmap]
rs11156974	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs11621735	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs11622986	0.96[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1170022	1.00[CEU][hapmap]
rs1170023	0.92[CEU][hapmap]
rs1170024	0.94[EUR][1000 genomes]
rs1170025	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1170028	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1170029	1.00[CEU][hapmap];0.92[CHB][hapmap];0.91[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1170030	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs1170031	0.89[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11851837	0.96[CEU][hapmap];0.81[CHB][hapmap]
rs12432452	1.00[CEU][hapmap]
rs12435640	0.96[CEU][hapmap];0.86[CHB][hapmap]
rs12590816	0.96[CEU][hapmap]
rs12882516	1.00[CEU][hapmap]
rs17107343	0.96[CEU][hapmap];0.92[CHB][hapmap];0.83[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17179919	0.96[CEU][hapmap];0.82[CHB][hapmap];0.82[EUR][1000 genomes]
rs17554993	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs1952787	0.96[CEU][hapmap];0.82[CHB][hapmap];0.82[EUR][1000 genomes]
rs1952788	0.96[CEU][hapmap]
rs1952790	0.81[CEU][hapmap]
rs1958693	1.00[CEU][hapmap]
rs1958694	0.96[CEU][hapmap]
rs1959676	1.00[CEU][hapmap]
rs2150322	0.96[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2183531	0.96[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2415421	0.80[EUR][1000 genomes]
rs3809444	0.96[CEU][hapmap]
rs4143919	0.96[CEU][hapmap]
rs4322573	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4597229	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs4898785	0.92[CEU][hapmap]
rs4901412	0.96[CEU][hapmap]
rs4901421	0.96[CEU][hapmap]
rs4901422	0.96[CEU][hapmap]
rs4901423	0.96[CEU][hapmap]
rs6571829	0.96[CEU][hapmap]
rs6571830	0.96[CEU][hapmap]
rs7153182	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7155891	0.96[CEU][hapmap]
rs7158383	0.96[EUR][1000 genomes]
rs8005651	1.00[CEU][hapmap]
rs8005895	0.96[CEU][hapmap]
rs8013747	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs8014454	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8014896	1.00[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8015738	1.00[CEU][hapmap]
rs8020796	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9322983	1.00[CEU][hapmap]
rs954881	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9788473	0.96[CEU][hapmap]
rs9788476	0.96[CEU][hapmap]

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	nsv916985	chr14:38052347-38838551	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
2	nsv564387	chr14:38357864-38563111	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv901651	chr14:38419360-38556242	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38440600-38442600	Weak transcription	Fetal Intestine Large	intestine
2	chr14:38440600-38442600	Weak transcription	Fetal Intestine Small	intestine
3	chr14:38441800-38443400	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr14:38442200-38443400	Enhancers	Duodenum Mucosa	Duodenum
5	chr14:38442200-38443400	Enhancers	HepG2	liver
6	chr14:38442200-38444400	Enhancers	Stomach Mucosa	stomach

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