Variant report

Variant	rs13199024
Chromosome Location	chr6:56734950-56734951
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:56722965..56725223-chr6:56732847..56735248,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs13190784	0.99[EUR][1000 genomes]
rs13191084	0.88[EUR][1000 genomes]
rs13195825	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13199233	0.87[EUR][1000 genomes]
rs13203600	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13205022	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13209099	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13212013	0.86[AFR][1000 genomes]
rs13216793	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16888192	0.81[EUR][1000 genomes]
rs17685045	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1870638	0.88[EUR][1000 genomes]
rs4443500	0.88[EUR][1000 genomes]
rs60563401	0.99[EUR][1000 genomes]
rs67063738	0.85[EUR][1000 genomes]
rs6905658	0.98[EUR][1000 genomes]
rs6911654	0.89[EUR][1000 genomes]
rs6925518	0.98[EUR][1000 genomes]
rs6926742	0.99[EUR][1000 genomes]
rs71564864	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73457800	0.82[EUR][1000 genomes]
rs7744240	0.87[EUR][1000 genomes]
rs7744799	0.87[EUR][1000 genomes]
rs9464401	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491933	chr6:56177722-57171010	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv934026	chr6:56382056-57184218	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv533050	chr6:56504480-57297586	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1021651	chr6:56569444-56966319	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv538228	chr6:56569444-56966319	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv1022714	chr6:56729767-56826642	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv538229	chr6:56729767-56826642	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv965728	chr6:56733888-56740633	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56728000-56735000	Enhancers	HSMM	muscle
2	chr6:56728000-56735000	Enhancers	NHDF-Ad	bronchial
3	chr6:56730400-56740400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr6:56732600-56736000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:56733800-56735200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr6:56734200-56755400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:56734400-56735000	Enhancers	GM12878-XiMat	blood
8	chr6:56734400-56735000	Enhancers	Osteobl	bone
9	chr6:56734400-56735200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:56734400-56735200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr6:56734400-56735600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:56734600-56750200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:56734600-56755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:56734800-56735000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:56734800-56740400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:56734800-56740400	Weak transcription	A549	lung
17	chr6:56734800-56740600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr6:56734800-56740600	Weak transcription	NHLF	lung
19	chr6:56734800-56754200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:56734800-56754400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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