Variant report

Variant	rs34818934
Chromosome Location	chr2:183597062-183597063
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:183579924..183582324-chr2:183596342..183598090,2	MCF-7	breast:
2	chr2:183596118..183599197-chr2:183620167..183622183,3	K562	blood:
3	chr2:183591742..183594215-chr2:183596337..183599496,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000077232	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1037404	0.85[EUR][1000 genomes]
rs11678585	0.87[EUR][1000 genomes]
rs11901549	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13509	0.85[EUR][1000 genomes]
rs167013	0.80[EUR][1000 genomes]
rs184078	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs190830	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs192618	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs208393	0.82[EUR][1000 genomes]
rs2118591	0.89[EUR][1000 genomes]
rs288239	0.85[EUR][1000 genomes]
rs288240	0.82[EUR][1000 genomes]
rs288241	0.85[EUR][1000 genomes]
rs288253	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288254	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288256	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288257	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288258	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288259	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288260	0.80[EUR][1000 genomes]
rs288263	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs288264	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs288265	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs288267	0.80[EUR][1000 genomes]
rs288268	0.80[EUR][1000 genomes]
rs288269	0.81[EUR][1000 genomes]
rs288278	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288280	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288283	0.83[EUR][1000 genomes]
rs288285	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288287	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs288289	0.85[ASN][1000 genomes]
rs288291	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288292	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288293	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288294	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288295	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288296	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288299	0.81[EUR][1000 genomes]
rs288300	0.83[EUR][1000 genomes]
rs288303	0.81[EUR][1000 genomes]
rs288304	0.85[EUR][1000 genomes]
rs288305	0.82[EUR][1000 genomes]
rs288306	0.85[EUR][1000 genomes]
rs288307	0.82[EUR][1000 genomes]
rs288308	0.82[EUR][1000 genomes]
rs288309	0.82[EUR][1000 genomes]
rs288310	0.82[EUR][1000 genomes]
rs288311	0.83[EUR][1000 genomes]
rs288312	0.86[EUR][1000 genomes]
rs288313	0.88[EUR][1000 genomes]
rs288331	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288332	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288334	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs288335	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs288336	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3115425	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs369573	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs409343	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs418159	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs418474	0.82[ASN][1000 genomes]
rs432527	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs438248	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs442044	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62188170	0.83[EUR][1000 genomes]
rs6745697	0.83[EUR][1000 genomes]
rs73975514	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs825660	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs825668	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9677291	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9678817	0.85[EUR][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	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2757842	chr2:183437700-183835084	Strong transcription Flanking Active TSS Weak transcription Enhancers 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 miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv2759104	chr2:183437700-183835084	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	esv2756954	chr2:183528670-183764930	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv875483	chr2:183537399-183657867	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	esv34847	chr2:183537399-183786763	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	esv3693445	chr2:183542825-183725221	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183581600-183609600	Weak transcription	Spleen	Spleen
2	chr2:183581800-183601200	Weak transcription	Colon Smooth Muscle	Colon
3	chr2:183581800-183601800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:183581800-183602000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr2:183581800-183606800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:183581800-183607000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:183581800-183614600	Weak transcription	Right Ventricle	heart
8	chr2:183581800-183622600	Weak transcription	Colonic Mucosa	Colon
9	chr2:183581800-183631000	Weak transcription	Esophagus	oesophagus
10	chr2:183581800-183647600	Weak transcription	Gastric	stomach
11	chr2:183581800-183655600	Weak transcription	Pancreas	Pancrea
12	chr2:183582000-183605200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr2:183582400-183601600	Weak transcription	Fetal Brain Female	brain
14	chr2:183582400-183601600	Weak transcription	Thymus	Thymus
15	chr2:183582400-183606800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr2:183582400-183608800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr2:183582400-183608800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr2:183582400-183610000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:183582600-183601600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:183582600-183601800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr2:183582600-183601800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr2:183582600-183602800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr2:183582600-183606800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr2:183582600-183606800	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr2:183582600-183608600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr2:183582600-183608800	Weak transcription	Fetal Heart	heart
27	chr2:183582600-183610600	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr2:183582600-183624400	Weak transcription	Stomach Mucosa	stomach
29	chr2:183582800-183601800	Weak transcription	NHLF	lung
30	chr2:183582800-183605200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr2:183582800-183610000	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr2:183582800-183610000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr2:183582800-183614600	Weak transcription	Fetal Brain Male	brain
34	chr2:183583000-183597600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:183583000-183601400	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr2:183583000-183605200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr2:183583000-183608400	Weak transcription	Hela-S3	cervix
38	chr2:183583200-183605400	Weak transcription	Brain Angular Gyrus	brain
39	chr2:183584000-183597600	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr2:183584200-183610400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr2:183584600-183597800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr2:183584800-183597600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr2:183584800-183598000	Strong transcription	NH-A	brain
44	chr2:183584800-183610200	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr2:183584800-183610400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:183584800-183610400	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr2:183586400-183601400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr2:183587000-183597200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:183588200-183606800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:183588200-183606800	Weak transcription	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links