Variant report

Variant	rs13336813
Chromosome Location	chr16:12097069-12097070
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	chr16:12070747..12072341-chr16:12096319..12098894,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260488	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs72784614	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8045634	0.82[CHB][hapmap]
rs8051278	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9939420	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042660	chr16:11846873-12110435	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv905347	chr16:12010444-12243329	Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
3	nsv1043096	chr16:12013915-12840769	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv482458	chr16:12014925-12145977	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1043959	chr16:12039346-12285269	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	nsv984259	chr16:12092609-12104575	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12071400-12130800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr16:12071800-12140200	Weak transcription	Fetal Intestine Small	intestine
3	chr16:12072200-12102600	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr16:12072400-12104400	Weak transcription	NHLF	lung
5	chr16:12072600-12099000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr16:12072800-12102800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr16:12079600-12109600	Weak transcription	Gastric	stomach
8	chr16:12083400-12102800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr16:12085400-12118200	Weak transcription	Esophagus	oesophagus
10	chr16:12088200-12100800	Weak transcription	Fetal Brain Female	brain
11	chr16:12088600-12098200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr16:12088600-12104200	Weak transcription	Right Ventricle	heart
13	chr16:12088600-12109200	Weak transcription	Fetal Kidney	kidney
14	chr16:12088600-12110000	Weak transcription	NH-A	brain
15	chr16:12088800-12098600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr16:12088800-12106600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr16:12088800-12108200	Weak transcription	Fetal Muscle Trunk	muscle
18	chr16:12088800-12115400	Weak transcription	Placenta	Placenta
19	chr16:12089000-12099800	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr16:12089000-12104400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr16:12089400-12103000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr16:12091000-12103000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr16:12091200-12098400	Weak transcription	Pancreas	Pancrea
24	chr16:12091400-12103000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr16:12091800-12101200	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr16:12092400-12105600	Weak transcription	Rectal Smooth Muscle	rectum
27	chr16:12092400-12110200	Weak transcription	NHEK	skin
28	chr16:12092600-12107800	Weak transcription	Liver	Liver
29	chr16:12092800-12098400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr16:12092800-12101200	Strong transcription	Primary B cells from peripheral blood	blood
31	chr16:12093200-12101600	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr16:12093200-12103800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr16:12093400-12102000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr16:12093400-12104000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr16:12093600-12098400	Strong transcription	Fetal Stomach	stomach
36	chr16:12093800-12103400	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr16:12094000-12103000	Weak transcription	Brain Substantia Nigra	brain
38	chr16:12094200-12098200	Weak transcription	Aorta	Aorta
39	chr16:12094200-12100800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr16:12094200-12103800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr16:12094200-12105600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr16:12094200-12110000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr16:12094800-12098600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr16:12094800-12098800	Weak transcription	Spleen	Spleen
45	chr16:12094800-12103000	Weak transcription	Brain Cingulate Gyrus	brain
46	chr16:12094800-12103000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr16:12094800-12104200	Weak transcription	Left Ventricle	heart
48	chr16:12095000-12103800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr16:12096000-12097200	Enhancers	Fetal Thymus	thymus
50	chr16:12096400-12097200	Enhancers	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links