Variant report

Variant	rs61344723
Chromosome Location	chr3:139992994-139992995
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:139991297..139993647-chr3:139995026..139996887,3	K562	blood:
2	chr3:139985294..139989044-chr3:139992240..139995969,3	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs55700145	1.00[EUR][1000 genomes]
rs55824862	1.00[EUR][1000 genomes]
rs55946470	1.00[EUR][1000 genomes]
rs56159033	1.00[EUR][1000 genomes]
rs56162195	1.00[EUR][1000 genomes]
rs56164954	1.00[EUR][1000 genomes]
rs57301721	1.00[EUR][1000 genomes]
rs60765002	1.00[EUR][1000 genomes]
rs6793849	1.00[EUR][1000 genomes]
rs72990136	1.00[EUR][1000 genomes]
rs72990139	1.00[EUR][1000 genomes]
rs72990140	1.00[EUR][1000 genomes]
rs72990146	1.00[EUR][1000 genomes]
rs72990147	1.00[EUR][1000 genomes]
rs72990154	1.00[EUR][1000 genomes]
rs72990157	1.00[EUR][1000 genomes]
rs72990159	1.00[EUR][1000 genomes]
rs72990160	1.00[EUR][1000 genomes]
rs72990162	1.00[EUR][1000 genomes]
rs72990164	1.00[EUR][1000 genomes]
rs72990166	1.00[EUR][1000 genomes]
rs7624775	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829739	chr3:139797496-140002685	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv432486	chr3:139924092-140049121	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2757891	chr3:139925764-140524730	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2759181	chr3:139925764-140524730	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv829740	chr3:139925767-140106169	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv527831	chr3:139932966-140533823	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139980200-139999400	Weak transcription	Pancreas	Pancrea
2	chr3:139991800-139993600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr3:139992200-139993200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr3:139992200-139993200	Bivalent Enhancer	HMEC	breast
5	chr3:139992400-139993000	Enhancers	NH-A	brain
6	chr3:139992400-139993200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:139992400-139994600	Weak transcription	HSMMtube	muscle
8	chr3:139992600-139993000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:139992600-139993000	Enhancers	NHEK	skin
10	chr3:139992600-139993200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:139992800-139993000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:139992800-139993000	Enhancers	H9 Cell Line	embryonic stem cell
13	chr3:139992800-139993200	Enhancers	Adipose Nuclei	Adipose

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