Variant report

Variant	rs700329
Chromosome Location	chr13:67798928-67798929
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	chr13:67263755..67264355-chr13:67798086..67798947,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12857493	0.92[ASN][1000 genomes]
rs1925750	0.81[ASN][1000 genomes]
rs1983871	0.87[ASN][1000 genomes]
rs1983949	0.83[ASN][1000 genomes]
rs2147998	0.87[ASN][1000 genomes]
rs2182229	0.85[ASN][1000 genomes]
rs2325025	0.90[ASN][1000 genomes]
rs2325027	0.90[ASN][1000 genomes]
rs3812859	0.87[ASN][1000 genomes]
rs3812860	0.88[ASN][1000 genomes]
rs4884719	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4884720	0.82[ASN][1000 genomes]
rs71427643	0.85[ASN][1000 genomes]
rs7489531	0.87[ASN][1000 genomes]
rs7992750	0.85[ASN][1000 genomes]
rs8002263	0.87[ASN][1000 genomes]
rs9317650	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9317651	0.85[ASN][1000 genomes]
rs9317655	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9529199	0.82[ASN][1000 genomes]
rs9529206	0.90[ASN][1000 genomes]
rs9541034	0.90[ASN][1000 genomes]
rs9541035	0.90[ASN][1000 genomes]
rs9571740	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035741	chr13:67212973-68077950	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv541817	chr13:67212973-68077950	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67794600-67800000	Active TSS	Fetal Brain Female	brain
2	chr13:67795400-67805600	Active TSS	Brain Substantia Nigra	brain
3	chr13:67795800-67799600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr13:67795800-67799800	Active TSS	Right Atrium	heart
5	chr13:67796000-67799600	Active TSS	Brain Hippocampus Middle	brain
6	chr13:67796000-67799600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr13:67796000-67799600	Active TSS	Stomach Smooth Muscle	stomach
8	chr13:67796200-67799400	Active TSS	Brain Anterior Caudate	brain
9	chr13:67796200-67799400	Active TSS	Brain Germinal Matrix	brain
10	chr13:67796200-67799600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr13:67796200-67799600	Weak transcription	Fetal Thymus	thymus
12	chr13:67796200-67799600	Active TSS	A549	lung
13	chr13:67796200-67801800	Weak transcription	Psoas Muscle	Psoas
14	chr13:67796200-67803000	Weak transcription	Gastric	stomach
15	chr13:67796200-67806000	Active TSS	Brain Inferior Temporal Lobe	brain
16	chr13:67796200-67806200	Active TSS	Brain Angular Gyrus	brain
17	chr13:67796400-67799400	Active TSS	Brain Cingulate Gyrus	brain
18	chr13:67797200-67799600	Active TSS	Fetal Brain Male	brain
19	chr13:67797200-67806000	Active TSS	Right Ventricle	heart
20	chr13:67797400-67799000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr13:67797400-67799600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr13:67797600-67806200	Active TSS	Fetal Kidney	kidney
23	chr13:67798000-67799400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr13:67798400-67799800	Enhancers	Fetal Heart	heart
25	chr13:67798400-67800400	Weak transcription	Fetal Muscle Trunk	muscle
26	chr13:67798600-67799000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr13:67798600-67799200	Enhancers	Primary B cells from cord blood	blood
28	chr13:67798600-67799400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr13:67798600-67799400	Weak transcription	Fetal Stomach	stomach
30	chr13:67798600-67799600	Weak transcription	Left Ventricle	heart
31	chr13:67798600-67799800	Enhancers	Dnd41	blood
32	chr13:67798600-67800000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr13:67798600-67801000	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr13:67798600-67801600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr13:67798600-67801600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr13:67798600-67801600	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr13:67798600-67802200	Weak transcription	Thymus	Thymus
38	chr13:67798600-67802200	Weak transcription	NH-A	brain
39	chr13:67798600-67802400	Weak transcription	HSMMtube	muscle
40	chr13:67798600-67802400	Weak transcription	NHDF-Ad	bronchial
41	chr13:67798600-67802600	Weak transcription	HUVEC	blood vessel
42	chr13:67798600-67802600	Weak transcription	Osteobl	bone
43	chr13:67798600-67802800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr13:67798600-67803000	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr13:67798600-67803200	Weak transcription	K562	blood
46	chr13:67798800-67799000	Active TSS	Muscle Satellite Cultured Cells	--
47	chr13:67798800-67799000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr13:67798800-67799200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr13:67798800-67799400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr13:67798800-67799400	Weak transcription	Primary B cells from peripheral blood	blood

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