Variant report

Variant	rs62176769
Chromosome Location	chr2:169721150-169721151
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10497345	0.97[EUR][1000 genomes]
rs10497348	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11893114	1.00[ASN][1000 genomes]
rs16823013	1.00[ASN][1000 genomes]
rs16856030	1.00[ASN][1000 genomes]
rs16856059	1.00[ASN][1000 genomes]
rs16856061	1.00[ASN][1000 genomes]
rs16856065	1.00[ASN][1000 genomes]
rs34073293	1.00[EUR][1000 genomes]
rs58191289	1.00[EUR][1000 genomes]
rs59686285	0.97[EUR][1000 genomes]
rs62175726	0.97[EUR][1000 genomes]
rs62176770	1.00[EUR][1000 genomes]
rs62176771	0.81[ASN][1000 genomes]
rs62176780	0.95[EUR][1000 genomes]
rs62176781	0.97[EUR][1000 genomes]
rs62176783	1.00[EUR][1000 genomes]
rs62176786	1.00[EUR][1000 genomes]
rs6739749	1.00[EUR][1000 genomes]
rs6739984	1.00[EUR][1000 genomes]
rs73014610	1.00[EUR][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	nsv583599	chr2:169664227-169903096	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv875381	chr2:169686559-169749841	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv516627	chr2:169714893-169721377	Strong transcription Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169689000-169721800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr2:169693400-169721400	Weak transcription	Spleen	Spleen
3	chr2:169693600-169721400	Weak transcription	Right Ventricle	heart
4	chr2:169698400-169721200	Weak transcription	Stomach Mucosa	stomach
5	chr2:169698600-169744600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:169702200-169721200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr2:169702200-169733000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:169702600-169721400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:169703600-169721200	Weak transcription	GM12878-XiMat	blood
10	chr2:169704200-169723400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:169704600-169721400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:169705000-169723600	Weak transcription	Fetal Brain Female	brain
13	chr2:169705200-169721400	Weak transcription	Fetal Kidney	kidney
14	chr2:169706600-169721600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr2:169706600-169727800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr2:169707400-169722000	Strong transcription	Rectal Mucosa Donor 31	rectum
17	chr2:169708600-169723200	Weak transcription	NHLF	lung
18	chr2:169708800-169721200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:169708800-169721200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:169708800-169721200	Weak transcription	A549	lung
21	chr2:169708800-169721200	Weak transcription	HMEC	breast
22	chr2:169709200-169721400	Weak transcription	HUVEC	blood vessel
23	chr2:169709400-169721200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:169709800-169733400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:169710200-169721200	Weak transcription	Fetal Lung	lung
26	chr2:169710200-169721400	Weak transcription	NHEK	skin
27	chr2:169710400-169721200	Strong transcription	K562	blood
28	chr2:169711400-169721600	Weak transcription	NH-A	brain
29	chr2:169712600-169721200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr2:169712600-169727800	Weak transcription	Primary T cells from cord blood	blood
31	chr2:169713200-169721200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr2:169713200-169728800	Weak transcription	Primary hematopoietic stem cells	blood
33	chr2:169713400-169721200	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr2:169713400-169721200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr2:169713400-169722000	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr2:169713400-169731200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr2:169713600-169722000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:169713800-169721200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr2:169714000-169732800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr2:169714200-169722000	Strong transcription	Dnd41	blood
41	chr2:169714400-169721400	Strong transcription	Adipose Nuclei	Adipose
42	chr2:169714400-169722200	Strong transcription	Duodenum Mucosa	Duodenum
43	chr2:169714800-169721200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:169715200-169721600	Strong transcription	Fetal Intestine Large	intestine
45	chr2:169715400-169721200	Weak transcription	HepG2	liver
46	chr2:169715400-169731600	Weak transcription	Small Intestine	intestine
47	chr2:169715400-169746200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:169716000-169722000	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr2:169716000-169745800	Weak transcription	HSMM	muscle
50	chr2:169717000-169722200	Strong transcription	Fetal Thymus	thymus

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