Variant report

Variant	rs2798147
Chromosome Location	chr1:210962447-210962448
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10863854	0.85[JPT][hapmap]
rs12022273	0.90[JPT][hapmap]
rs1317255	0.85[JPT][hapmap]
rs1340127	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs1340128	0.90[JPT][hapmap]
rs1343143	0.83[EUR][1000 genomes]
rs1343147	0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs1770213	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs1770215	0.85[JPT][hapmap]
rs1770216	0.90[EUR][1000 genomes]
rs1770218	0.84[ASN][1000 genomes]
rs1770219	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1770220	0.90[CHB][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs1770221	0.94[CEU][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1770222	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1777243	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1777245	0.93[CEU][hapmap];0.86[EUR][1000 genomes]
rs1777246	0.87[EUR][1000 genomes]
rs1777247	0.86[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs1777252	0.90[JPT][hapmap]
rs1777254	0.85[JPT][hapmap]
rs1777255	0.85[JPT][hapmap]
rs1777256	0.85[JPT][hapmap]
rs1777257	0.84[JPT][hapmap]
rs1777258	0.92[EUR][1000 genomes]
rs1777259	0.86[ASN][1000 genomes]
rs1777260	0.92[EUR][1000 genomes]
rs1777264	0.93[CEU][hapmap];0.86[EUR][1000 genomes]
rs1890840	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1934632	0.85[JPT][hapmap]
rs1934633	0.90[JPT][hapmap]
rs2798145	0.80[ASN][1000 genomes]
rs4282878	0.85[JPT][hapmap]
rs4951615	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs4951640	0.94[CEU][hapmap];0.85[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6658580	0.82[CEU][hapmap];0.83[EUR][1000 genomes]
rs6666042	0.94[CEU][hapmap];0.83[EUR][1000 genomes]
rs7515909	0.94[CEU][hapmap]
rs7546472	0.88[CEU][hapmap]
rs9429845	0.85[JPT][hapmap]

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	nsv873148	chr1:210665583-210994339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv873153	chr1:210900481-210994339	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv999018	chr1:210907239-210999306	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv832503	chr1:210948760-211103163	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210941800-210978000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:210944400-210965800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:210946800-210965800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr1:210953400-210974400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr1:210955200-210965400	Weak transcription	Brain Angular Gyrus	brain
6	chr1:210961200-210964200	Strong transcription	HSMM	muscle
7	chr1:210962400-210964000	Strong transcription	HSMMtube	muscle

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