Variant report

Variant	rs56984047
Chromosome Location	chr16:31899523-31899524
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	chr16:31897518..31899829-chr16:31901532..31903567,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs57664662	0.93[AFR][1000 genomes]
rs58487380	1.00[AFR][1000 genomes]
rs58641712	0.93[AFR][1000 genomes]
rs59378014	0.93[AFR][1000 genomes]
rs61394714	0.93[AFR][1000 genomes]
rs952006	1.00[AFR][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	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv918074	chr16:31669781-31935033	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv1063037	chr16:31669981-31934894	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv542903	chr16:31669981-31934894	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1066522	chr16:31831196-31959992	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers 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	26 gene(s)	inside rSNPs	diseases
6	nsv1057300	chr16:31862900-31959992	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv833196	chr16:31897381-32068953	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31886800-31901000	Weak transcription	Fetal Brain Male	brain
2	chr16:31887000-31901600	Weak transcription	Fetal Brain Female	brain
3	chr16:31887000-31902200	ZNF genes & repeats	A549	lung
4	chr16:31887200-31900800	Weak transcription	Brain Germinal Matrix	brain
5	chr16:31887400-31900800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr16:31887800-31907400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr16:31889400-31911600	ZNF genes & repeats	Primary B cells from cord blood	blood
8	chr16:31890200-31905800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr16:31891800-31901800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr16:31892000-31900800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr16:31892000-31905000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr16:31892000-31910400	ZNF genes & repeats	GM12878-XiMat	blood
13	chr16:31892200-31900800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr16:31892200-31901600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr16:31892200-31905000	Weak transcription	Fetal Heart	heart
16	chr16:31892400-31899600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
17	chr16:31892400-31903400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr16:31892400-31904200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr16:31892400-31905000	Weak transcription	Brain Substantia Nigra	brain
20	chr16:31892400-31905800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr16:31892800-31900800	Weak transcription	Ovary	ovary
22	chr16:31892800-31901600	Weak transcription	Brain Anterior Caudate	brain
23	chr16:31892800-31902600	Weak transcription	Pancreas	Pancrea
24	chr16:31892800-31905200	Weak transcription	Right Ventricle	heart
25	chr16:31892800-31906000	Weak transcription	Psoas Muscle	Psoas
26	chr16:31893000-31900800	Strong transcription	Primary B cells from peripheral blood	blood
27	chr16:31893000-31913200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr16:31893200-31911800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr16:31893400-31902800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr16:31893400-31911400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr16:31893400-31911800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr16:31893400-31912000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
33	chr16:31893600-31917800	Weak transcription	Colon Smooth Muscle	Colon
34	chr16:31893800-31903400	Strong transcription	HSMM	muscle
35	chr16:31894000-31903000	Weak transcription	Stomach Mucosa	stomach
36	chr16:31894800-31900000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr16:31895000-31901000	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr16:31895000-31908400	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr16:31895000-31909600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chr16:31895200-31899600	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr16:31895200-31899800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr16:31895200-31900200	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr16:31895200-31900600	Strong transcription	Liver	Liver
44	chr16:31895200-31901200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr16:31895200-31901600	Strong transcription	HUVEC	blood vessel
46	chr16:31895200-31901800	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr16:31895200-31902400	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr16:31895400-31899600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr16:31895600-31901000	Strong transcription	HepG2	liver
50	chr16:31895800-31910200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links