Variant report

Variant	rs13396130
Chromosome Location	chr2:145588603-145588604
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:145566900..145569050-chr2:145586753..145589174,2	K562	blood:
2	chr2:145577953..145579496-chr2:145588268..145589798,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10181009	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10196836	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1038363	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1085460	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1085461	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1092395	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10928230	0.88[ASN][1000 genomes]
rs11899456	0.95[ASN][1000 genomes]
rs11902294	0.82[JPT][hapmap]
rs12623452	0.84[JPT][hapmap]
rs13018654	0.94[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13028678	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1384781	0.88[ASN][1000 genomes]
rs1528186	0.97[ASN][1000 genomes]
rs2381663	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35099259	0.84[JPT][hapmap]
rs3856365	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs60111010	0.80[ASN][1000 genomes]
rs706624	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs706625	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs786486	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs786487	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs786489	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786490	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs786492	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs786493	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs786494	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs786495	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs786498	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs786499	0.98[ASN][1000 genomes]
rs786500	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs786502	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9646654	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs987762	0.81[AMR][1000 genomes];0.99[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	nsv1002563	chr2:145182201-145863253	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv535957	chr2:145182201-145863253	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv834397	chr2:145439528-145608628	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv932113	chr2:145515124-145844491	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:145583600-145589600	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr2:145584000-145589200	Weak transcription	K562	blood
3	chr2:145587600-145589200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:145587800-145591400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr2:145588000-145589000	Enhancers	NHLF	lung
6	chr2:145588000-145589400	Enhancers	NHDF-Ad	bronchial
7	chr2:145588200-145589600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr2:145588400-145592000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:145588400-145592600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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