Variant report

Variant	rs4585566
Chromosome Location	chr6:56400460-56400461
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:56398077..56400962-chr6:56401619..56403800,2	K562	blood:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs17830661	0.92[AFR][1000 genomes]
rs56273018	0.88[AFR][1000 genomes]
rs56851245	0.96[AFR][1000 genomes]
rs57822928	0.92[AFR][1000 genomes]
rs58633665	1.00[AFR][1000 genomes]
rs59063378	0.92[AFR][1000 genomes]
rs59948116	1.00[AFR][1000 genomes]
rs73455767	0.92[AFR][1000 genomes]
rs73455787	0.83[AFR][1000 genomes]
rs73749957	1.00[AFR][1000 genomes]
rs73749958	1.00[AFR][1000 genomes]
rs73749960	1.00[AFR][1000 genomes]
rs73749980	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv830666	chr6:56243743-56419599	Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv885912	chr6:56327849-56458836	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1016868	chr6:56376165-56417631	Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	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

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56341800-56407400	Weak transcription	Spleen	Spleen
2	chr6:56363000-56402200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:56376400-56407200	Weak transcription	Gastric	stomach
4	chr6:56377200-56404200	Weak transcription	K562	blood
5	chr6:56380600-56401200	Weak transcription	Psoas Muscle	Psoas
6	chr6:56383200-56402400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:56384400-56402200	Weak transcription	Small Intestine	intestine
8	chr6:56388000-56402200	Strong transcription	Fetal Intestine Large	intestine
9	chr6:56388200-56401800	Strong transcription	Liver	Liver
10	chr6:56390200-56401400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:56390200-56401600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:56390600-56403800	Weak transcription	Thymus	Thymus
13	chr6:56390800-56402400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:56390800-56403000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:56391400-56400800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr6:56391400-56400800	Weak transcription	Esophagus	oesophagus
17	chr6:56391400-56400800	Weak transcription	Right Ventricle	heart
18	chr6:56391400-56401200	Weak transcription	Right Atrium	heart
19	chr6:56391400-56402200	Weak transcription	Lung	lung
20	chr6:56391400-56402400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:56391400-56402800	Strong transcription	Fetal Muscle Leg	muscle
22	chr6:56392000-56400800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr6:56392200-56401600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:56392400-56401600	Strong transcription	Adipose Nuclei	Adipose
25	chr6:56392400-56406200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr6:56393000-56401400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr6:56393000-56402000	Weak transcription	Fetal Heart	heart
28	chr6:56393600-56400600	Weak transcription	Fetal Brain Male	brain
29	chr6:56394800-56400800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:56394800-56401000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:56395000-56401400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:56395400-56401200	Strong transcription	Muscle Satellite Cultured Cells	--
33	chr6:56395400-56401200	Strong transcription	NHDF-Ad	bronchial
34	chr6:56395400-56405200	Weak transcription	Placenta	Placenta
35	chr6:56395600-56401200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:56395800-56401200	Strong transcription	Osteobl	bone
37	chr6:56396000-56401200	Strong transcription	HSMMtube	muscle
38	chr6:56396200-56401400	Strong transcription	HepG2	liver
39	chr6:56396400-56401200	Strong transcription	NH-A	brain
40	chr6:56396800-56401600	Strong transcription	HMEC	breast
41	chr6:56396800-56401800	Genic enhancers	Colon Smooth Muscle	Colon
42	chr6:56397000-56400600	Weak transcription	Aorta	Aorta
43	chr6:56397000-56401600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:56397000-56403600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr6:56397000-56405200	Weak transcription	Brain Germinal Matrix	brain
46	chr6:56397200-56400800	Weak transcription	Hela-S3	cervix
47	chr6:56397200-56402200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:56397200-56406600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr6:56397400-56405600	Weak transcription	Fetal Brain Female	brain
50	chr6:56398200-56401200	Weak transcription	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links