Variant report

Variant	rs3843323
Chromosome Location	chr2:180856459-180856460
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:180855717..180856981-chr2:180941679..180942512,4	MCF-7	breast:
2	chr2:180854973..180857186-chr2:180866635..180869075,2	MCF-7	breast:
3	chr2:180856151..180858143-chr2:180858684..180861516,4	K562	blood:
4	chr2:180856098..180856777-chr2:180941779..180942671,2	K562	blood:
5	chr2:180828665..180830720-chr2:180855146..180856897,2	MCF-7	breast:
6	chr2:180853987..180858139-chr2:180866524..180870001,3	MCF-7	breast:
7	chr2:180854938..180857526-chr2:180942782..180945485,2	MCF-7	breast:
8	chr2:180856164..180859331-chr2:180861905..180864411,3	K562	blood:

No data

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12465592	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12468986	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12693214	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12693215	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16867131	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1904850	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2367990	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs259810	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs259811	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2678936	1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3845701	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3856415	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs56401468	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6433816	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6433818	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6433820	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6433821	1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6722147	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6727890	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6733426	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6744281	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6759271	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72958863	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72960660	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72960664	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72960701	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72962517	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72962575	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs818661	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9288045	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][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	nsv875472	chr2:180696414-181024926	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv875473	chr2:180696414-181055597	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1006598	chr2:180766983-180923051	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv531444	chr2:180796233-181434590	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS 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:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180807000-180858400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr2:180808200-180860400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:180809400-180871000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:180813400-180868200	Weak transcription	Stomach Mucosa	stomach
5	chr2:180816800-180860400	Weak transcription	Right Ventricle	heart
6	chr2:180816800-180868400	Weak transcription	Pancreas	Pancrea
7	chr2:180816800-180869000	Weak transcription	Spleen	Spleen
8	chr2:180816800-180870600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr2:180817200-180860400	Weak transcription	Aorta	Aorta
10	chr2:180817200-180860400	Weak transcription	Gastric	stomach
11	chr2:180819000-180871000	Weak transcription	Esophagus	oesophagus
12	chr2:180821600-180858800	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr2:180822200-180858200	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr2:180823400-180870600	Weak transcription	Fetal Intestine Small	intestine
15	chr2:180829600-180871200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:180830200-180857600	Weak transcription	Fetal Heart	heart
17	chr2:180830800-180871000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr2:180831000-180860400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr2:180832800-180860200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:180834200-180858200	Strong transcription	Primary B cells from cord blood	blood
21	chr2:180836800-180870400	Weak transcription	A549	lung
22	chr2:180839800-180870400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr2:180840600-180858200	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr2:180840600-180858200	Strong transcription	Dnd41	blood
25	chr2:180841000-180858200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:180843000-180870200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr2:180846800-180867000	Weak transcription	Colon Smooth Muscle	Colon
28	chr2:180846800-180869800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:180847600-180866200	Weak transcription	Psoas Muscle	Psoas
30	chr2:180848400-180858200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:180849000-180856600	Weak transcription	Fetal Brain Male	brain
32	chr2:180849000-180858200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr2:180849000-180869600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr2:180850400-180862200	Weak transcription	Small Intestine	intestine
35	chr2:180850600-180870800	Weak transcription	HSMMtube	muscle
36	chr2:180851000-180870200	Weak transcription	Hela-S3	cervix
37	chr2:180851600-180870400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr2:180851800-180857200	Weak transcription	Brain Substantia Nigra	brain
39	chr2:180851800-180870400	Weak transcription	HUVEC	blood vessel
40	chr2:180852000-180857400	Weak transcription	NH-A	brain
41	chr2:180852000-180859200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr2:180852000-180860600	Weak transcription	Brain Hippocampus Middle	brain
43	chr2:180852000-180865000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr2:180852200-180856800	Weak transcription	Fetal Kidney	kidney
45	chr2:180852200-180857200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr2:180852200-180857600	Weak transcription	Brain Angular Gyrus	brain
47	chr2:180852200-180857600	Weak transcription	HMEC	breast
48	chr2:180852200-180870600	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr2:180852400-180857600	Weak transcription	HSMM	muscle
50	chr2:180852400-180860400	Weak transcription	H1 Cell Line	embryonic stem cell

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