Variant report

Variant	rs73479216
Chromosome Location	chr13:49061442-49061443
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:49058648..49060193-chr13:49061101..49062675,2	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs12583617	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12583644	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12583787	0.83[ASN][1000 genomes]
rs12585384	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12585742	1.00[EUR][1000 genomes]
rs12857866	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17071937	0.83[ASN][1000 genomes]
rs2148515	0.83[ASN][1000 genomes]
rs3092898	0.97[AFR][1000 genomes]
rs4151472	1.00[EUR][1000 genomes]
rs4151479	1.00[EUR][1000 genomes]
rs4151524	1.00[EUR][1000 genomes]
rs4151598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4151602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4151613	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs449268	0.83[ASN][1000 genomes]
rs55686933	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57394470	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6650379	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7139763	0.83[ASN][1000 genomes]
rs7319276	0.83[ASN][1000 genomes]
rs7326934	0.83[ASN][1000 genomes]
rs73479220	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73495016	0.87[AFR][1000 genomes]
rs73495018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73495037	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs74074915	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs74074916	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs74074942	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs74074944	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs74074946	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs74074951	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs74077638	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9316384	0.83[ASN][1000 genomes]
rs9316386	0.83[ASN][1000 genomes]
rs9316387	0.83[ASN][1000 genomes]
rs9316396	0.83[ASN][1000 genomes]
rs9316398	0.83[ASN][1000 genomes]
rs9331984	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9331994	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9332033	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9332044	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9332055	0.83[ASN][1000 genomes]
rs9332070	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9332085	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9591176	0.83[ASN][1000 genomes]
rs9595914	0.83[ASN][1000 genomes]
rs9595924	0.83[ASN][1000 genomes]
rs9595926	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832602	chr13:49003159-49167781	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv1041275	chr13:49045566-49242357	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv541769	chr13:49045566-49242357	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv832604	chr13:49061081-49281807	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 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	chr13:49017400-49062200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr13:49018000-49062400	Weak transcription	Fetal Brain Male	brain
3	chr13:49020800-49062000	Weak transcription	Fetal Kidney	kidney
4	chr13:49023800-49073800	Weak transcription	NH-A	brain
5	chr13:49025600-49066200	Weak transcription	Psoas Muscle	Psoas
6	chr13:49028000-49071000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr13:49029200-49062000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr13:49030600-49070600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr13:49031600-49066200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr13:49031800-49065400	Weak transcription	Brain Substantia Nigra	brain
11	chr13:49032000-49065600	Weak transcription	Brain Anterior Caudate	brain
12	chr13:49032000-49066200	Weak transcription	Colonic Mucosa	Colon
13	chr13:49032400-49062600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr13:49032400-49066200	Weak transcription	Spleen	Spleen
15	chr13:49032400-49066600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr13:49032400-49066600	Weak transcription	Ovary	ovary
17	chr13:49032400-49067400	Weak transcription	Pancreas	Pancrea
18	chr13:49032400-49067600	Weak transcription	Gastric	stomach
19	chr13:49032800-49066200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr13:49034400-49073800	Weak transcription	Esophagus	oesophagus
21	chr13:49035200-49073400	Weak transcription	Fetal Intestine Small	intestine
22	chr13:49035600-49065400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr13:49035600-49066000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr13:49035800-49061800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr13:49035800-49066400	Weak transcription	NHEK	skin
26	chr13:49039800-49062000	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr13:49049600-49062200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr13:49049800-49066200	Weak transcription	Lung	lung
29	chr13:49050000-49061800	Weak transcription	Fetal Brain Female	brain
30	chr13:49050000-49065600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr13:49051200-49063600	Weak transcription	Primary T cells from cord blood	blood
32	chr13:49051200-49064800	Weak transcription	Brain Hippocampus Middle	brain
33	chr13:49051800-49065400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr13:49052000-49062000	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr13:49052800-49063600	Weak transcription	Adipose Nuclei	Adipose
36	chr13:49052800-49064800	Weak transcription	Liver	Liver
37	chr13:49053200-49063800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr13:49053600-49063200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr13:49053600-49071200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr13:49053800-49066600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr13:49054000-49094000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:49054200-49062400	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr13:49054200-49064800	Weak transcription	Thymus	Thymus
44	chr13:49054200-49066600	Weak transcription	Aorta	Aorta
45	chr13:49054400-49062000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr13:49054400-49062000	Weak transcription	Fetal Lung	lung
47	chr13:49054400-49062400	Weak transcription	Fetal Intestine Large	intestine
48	chr13:49054400-49062400	Weak transcription	Left Ventricle	heart
49	chr13:49054400-49062600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr13:49054400-49063800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links