Variant report

Variant	rs60962957
Chromosome Location	chr6:56753505-56753506
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11963379	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11965554	1.00[AMR][1000 genomes]
rs11969595	1.00[AMR][1000 genomes]
rs28432154	1.00[AMR][1000 genomes]
rs59524770	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60547490	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60910643	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9464406	0.83[AMR][1000 genomes]
rs9464408	1.00[AMR][1000 genomes]
rs9475742	1.00[AMR][1000 genomes]
rs9475743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9475745	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9475746	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9475750	1.00[AMR][1000 genomes]
rs9475751	0.83[AMR][1000 genomes]
rs9475754	1.00[AMR][1000 genomes]
rs9475755	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	nsv508408	chr6:56735681-56773285	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv5315	chr6:56752042-56798761	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56734200-56755400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:56734600-56755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:56734800-56754200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:56734800-56754400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:56736400-56755800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:56741200-56754600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr6:56741600-56754200	Weak transcription	NHLF	lung
8	chr6:56743600-56753800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:56749200-56769600	Weak transcription	Brain Angular Gyrus	brain
10	chr6:56750400-56753600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:56750600-56754400	Weak transcription	Osteobl	bone
12	chr6:56750800-56754600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:56751000-56754600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:56751200-56753800	Weak transcription	NHDF-Ad	bronchial
15	chr6:56751800-56753600	Enhancers	Primary T cells from cord blood	blood
16	chr6:56752000-56754800	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr6:56752200-56754800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:56752200-56754800	Weak transcription	HSMM	muscle
19	chr6:56752400-56767000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr6:56752600-56753600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:56752600-56754200	Weak transcription	HSMMtube	muscle
22	chr6:56752600-56754400	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr6:56752600-56755000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr6:56752800-56754600	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr6:56753000-56754600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr6:56753000-56755600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:56753200-56753800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr6:56753200-56753800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr6:56753200-56753800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:56753200-56753800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:56753200-56755000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr6:56753200-56756200	Enhancers	HUVEC	blood vessel
33	chr6:56753400-56754200	Enhancers	A549	lung
34	chr6:56753400-56754200	Enhancers	GM12878-XiMat	blood

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