Variant report

Variant	rs2560750
Chromosome Location	chr6:13467019-13467020
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:13466304..13467866-chr6:13471367..13474038,2	K562	blood:
2	chr6:13460797..13463308-chr6:13464460..13467196,3	K562	blood:
3	chr6:13465251..13472690-chr6:13481619..13489131,10	K562	blood:
4	chr6:13466729..13469720-chr6:13485556..13487664,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000237786	Chromatin interaction
ENSG00000187461	Chromatin interaction
ENSG00000145990	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11964734	1.00[AMR][1000 genomes]
rs2434393	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2434394	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2494771	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2560751	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2560752	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2560753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2560816	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2560817	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2560818	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2841553	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2841554	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2841556	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2841557	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2841558	0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2841559	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58453010	0.83[AMR][1000 genomes]
rs59772696	1.00[AMR][1000 genomes]
rs6931785	1.00[AMR][1000 genomes]
rs73725831	1.00[AMR][1000 genomes]
rs766773	0.84[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7774411	0.83[AMR][1000 genomes]
rs9382115	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532021	chr6:13232627-13805381	Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv1028533	chr6:13239059-13484814	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv538136	chr6:13239059-13484814	Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1033620	chr6:13419730-13571788	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv462640	chr6:13426539-13519434	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv600994	chr6:13426539-13519434	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv470802	chr6:13441424-13519371	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13452200-13483400	Weak transcription	Gastric	stomach
2	chr6:13454400-13485000	Weak transcription	Colonic Mucosa	Colon
3	chr6:13455200-13484400	Weak transcription	Small Intestine	intestine
4	chr6:13455200-13484600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr6:13455400-13481000	Weak transcription	HUVEC	blood vessel
6	chr6:13456600-13467200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:13461800-13468000	Enhancers	NHLF	lung
8	chr6:13462600-13470200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:13462800-13484800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr6:13463000-13468200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr6:13463000-13468200	Enhancers	Psoas Muscle	Psoas
12	chr6:13463000-13470800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr6:13463200-13468800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:13463200-13481000	Weak transcription	A549	lung
15	chr6:13463400-13467800	Weak transcription	Liver	Liver
16	chr6:13463400-13476600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr6:13463600-13470200	Weak transcription	Osteobl	bone
18	chr6:13463600-13470400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:13463600-13470600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:13463600-13473200	Weak transcription	HepG2	liver
21	chr6:13463600-13484400	Weak transcription	Primary T cells from cord blood	blood
22	chr6:13463800-13484600	Weak transcription	Duodenum Mucosa	Duodenum
23	chr6:13464400-13467400	Enhancers	Primary B cells from peripheral blood	blood
24	chr6:13464400-13468000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:13464600-13468600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:13464600-13469000	Weak transcription	Lung	lung
27	chr6:13464600-13469200	Weak transcription	Brain Substantia Nigra	brain
28	chr6:13464600-13470400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:13464600-13476400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:13464800-13468800	Weak transcription	Aorta	Aorta
31	chr6:13465000-13467200	Enhancers	Primary B cells from cord blood	blood
32	chr6:13465000-13467800	Enhancers	Brain Anterior Caudate	brain
33	chr6:13465200-13485000	Weak transcription	Rectal Smooth Muscle	rectum
34	chr6:13465400-13467200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:13465600-13467200	Enhancers	Right Atrium	heart
36	chr6:13465600-13467200	Enhancers	HMEC	breast
37	chr6:13465600-13467400	Enhancers	Spleen	Spleen
38	chr6:13465600-13467800	Enhancers	Brain Hippocampus Middle	brain
39	chr6:13465600-13468000	Enhancers	Stomach Smooth Muscle	stomach
40	chr6:13465800-13467200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:13465800-13467400	Enhancers	Adipose Nuclei	Adipose
42	chr6:13465800-13467800	Enhancers	Primary hematopoietic stem cells	blood
43	chr6:13465800-13467800	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr6:13465800-13467800	Enhancers	HSMM	muscle
45	chr6:13465800-13468200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:13465800-13470200	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr6:13466000-13467200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:13466000-13467400	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr6:13466000-13470200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr6:13466200-13467200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links