Variant report

Variant	rs4670145
Chromosome Location	chr2:36627725-36627726
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	chr2:36621514..36623196-chr2:36625888..36628234,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10184188	0.81[ASN][1000 genomes]
rs11885390	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11891181	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12712499	0.91[JPT][hapmap]
rs12712501	0.91[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs34582671	0.90[ASN][1000 genomes]
rs3770911	0.92[CHB][hapmap];0.89[CHD][hapmap];0.84[JPT][hapmap];0.87[ASN][1000 genomes]
rs3770912	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3770919	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3770928	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3770935	0.94[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3770938	0.82[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs3770939	0.91[CHB][hapmap];0.94[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3770941	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3770943	0.92[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3770949	1.00[JPT][hapmap]
rs3821162	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4670553	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67044425	0.90[ASN][1000 genomes]
rs72785173	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833803	chr2:36589065-36745779	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2756915	chr2:36622906-36657305	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2759041	chr2:36622906-36657305	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36604400-36640400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr2:36604400-36640600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr2:36611600-36632400	Weak transcription	Esophagus	oesophagus
4	chr2:36611600-36635400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:36616800-36631200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:36616800-36635000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:36617000-36633400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr2:36617200-36630800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr2:36617200-36631200	Weak transcription	Fetal Kidney	kidney
10	chr2:36617200-36633800	Weak transcription	Fetal Lung	lung
11	chr2:36617800-36630600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr2:36617800-36630600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:36618600-36643000	Genic enhancers	Osteobl	bone
14	chr2:36620200-36635000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:36620800-36629200	Genic enhancers	Muscle Satellite Cultured Cells	--
16	chr2:36621000-36630600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr2:36621000-36631400	Weak transcription	Fetal Brain Female	brain
18	chr2:36621000-36635000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr2:36621000-36635200	Weak transcription	Lung	lung
20	chr2:36621200-36628000	Weak transcription	Ovary	ovary
21	chr2:36621200-36629000	Weak transcription	Fetal Muscle Leg	muscle
22	chr2:36621200-36630800	Weak transcription	Spleen	Spleen
23	chr2:36621200-36634800	Weak transcription	Brain Hippocampus Middle	brain
24	chr2:36621200-36634800	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr2:36621200-36635000	Weak transcription	Fetal Stomach	stomach
26	chr2:36622600-36628000	Genic enhancers	NHDF-Ad	bronchial
27	chr2:36622600-36630600	Genic enhancers	HUVEC	blood vessel
28	chr2:36622800-36629000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:36622800-36629400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:36622800-36630600	Weak transcription	Colon Smooth Muscle	Colon
31	chr2:36622800-36631400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr2:36623000-36632200	Weak transcription	Right Atrium	heart
33	chr2:36623400-36629600	Strong transcription	Placenta	Placenta
34	chr2:36623600-36630800	Genic enhancers	NHLF	lung
35	chr2:36624000-36631400	Enhancers	Psoas Muscle	Psoas
36	chr2:36624200-36629600	Genic enhancers	Skeletal Muscle Female	skeletal muscle
37	chr2:36624200-36635000	Weak transcription	Brain Angular Gyrus	brain
38	chr2:36624400-36627800	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr2:36624400-36628000	Strong transcription	HMEC	breast
40	chr2:36624400-36628600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr2:36624400-36630800	Weak transcription	Small Intestine	intestine
42	chr2:36624600-36628200	Strong transcription	NHEK	skin
43	chr2:36624600-36630400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr2:36624600-36630800	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr2:36624600-36634600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:36624800-36643600	Weak transcription	Colonic Mucosa	Colon
47	chr2:36625200-36629000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr2:36625200-36635000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:36625400-36629000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr2:36625400-36630800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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