Variant report

Variant	rs12133238
Chromosome Location	chr1:150165860-150165861
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:150158453..150162673-chr1:150163333..150168341,4	K562	blood:
2	chr1:149857548..149860200-chr1:150165414..150168428,4	K562	blood:
3	chr1:150164304..150165921-chr1:150174618..150176672,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000184260	Chromatin interaction
ENSG00000184678	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000184270	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10788872	0.84[ASN][1000 genomes]
rs10888574	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10888575	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10888576	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11205339	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11205340	0.99[ASN][1000 genomes]
rs11205341	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs11205343	0.94[ASN][1000 genomes]
rs11205347	0.88[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11205348	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11811787	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12131063	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12133235	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12136311	0.83[EUR][1000 genomes]
rs12569047	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1535873	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1924549	0.91[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs2038752	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2038753	0.94[ASN][1000 genomes]
rs3118124	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3121000	0.94[ASN][1000 genomes]
rs3121001	0.99[ASN][1000 genomes]
rs3754048	0.81[CEU][hapmap]
rs3850839	0.82[CEU][hapmap]
rs4408187	0.99[ASN][1000 genomes]
rs55647200	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55956539	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59507173	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61161619	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6587753	0.94[ASN][1000 genomes]
rs6655935	0.90[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs6660127	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6665499	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6680040	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6682434	0.98[ASN][1000 genomes]
rs6692738	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6694215	0.94[ASN][1000 genomes]
rs6703332	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7522034	0.95[JPT][hapmap]
rs7532164	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7535712	0.88[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.89[EUR][1000 genomes]
rs7548543	0.90[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7550600	0.95[EUR][1000 genomes]
rs7551023	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7555995	0.94[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[EUR][1000 genomes];0.92[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	nsv529719	chr1:150006344-150311095	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	nsv535153	chr1:150147218-150168829	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150160200-150166600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:150164200-150166000	Enhancers	Osteobl	bone
3	chr1:150164200-150166800	Enhancers	NH-A	brain
4	chr1:150164800-150166000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:150164800-150166000	Enhancers	Fetal Heart	heart
6	chr1:150165000-150166600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:150165000-150166600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr1:150165000-150166600	Weak transcription	NHDF-Ad	bronchial
9	chr1:150165000-150166800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:150165000-150166800	Weak transcription	NHLF	lung
11	chr1:150165200-150166400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:150165200-150166600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:150165200-150166800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:150165600-150166600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr1:150165600-150166600	Weak transcription	HSMMtube	muscle
16	chr1:150165600-150166800	Weak transcription	A549	lung
17	chr1:150165800-150166800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:150165800-150166800	Weak transcription	HSMM	muscle

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