Variant report

Variant	rs3769150
Chromosome Location	chr2:174099591-174099592
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:174091632..174094180-chr2:174097237..174099910,2	MCF-7	breast:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10169914	0.96[CHB][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12996371	1.00[CEU][hapmap]
rs16861406	0.87[CHB][hapmap];0.84[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs16861417	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs16861422	0.83[CHB][hapmap]
rs16861423	0.82[CHB][hapmap]
rs2119123	0.91[CHB][hapmap];0.83[ASN][1000 genomes]
rs3739103	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3754737	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs3754738	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3769151	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3769152	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3769154	0.95[CHB][hapmap];0.91[ASN][1000 genomes]
rs3820831	0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs3820832	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs41268713	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4972538	0.95[CHB][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72625241	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs72625242	0.97[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7560960	1.00[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011724	chr2:173916482-174231908	Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:174058000-174112800	Weak transcription	Spleen	Spleen
2	chr2:174083400-174100600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:174083400-174136400	Weak transcription	Esophagus	oesophagus
4	chr2:174083600-174103400	Weak transcription	NHLF	lung
5	chr2:174083800-174119200	Weak transcription	HMEC	breast
6	chr2:174086200-174101600	Weak transcription	Ovary	ovary
7	chr2:174089600-174103000	Weak transcription	K562	blood
8	chr2:174092200-174109400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:174092400-174100600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr2:174092400-174100600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:174092400-174101200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:174092800-174101200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr2:174092800-174109200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr2:174093000-174101200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr2:174093000-174102600	Weak transcription	Fetal Lung	lung
16	chr2:174093800-174106800	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr2:174094200-174100800	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr2:174094800-174114600	Weak transcription	HUVEC	blood vessel
19	chr2:174095800-174102800	Strong transcription	Fetal Stomach	stomach
20	chr2:174096000-174128800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr2:174096200-174100200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:174096200-174100800	Weak transcription	Primary B cells from peripheral blood	blood
23	chr2:174096200-174102400	Weak transcription	Stomach Mucosa	stomach
24	chr2:174096200-174118200	Weak transcription	Rectal Smooth Muscle	rectum
25	chr2:174096400-174100200	Weak transcription	Brain Germinal Matrix	brain
26	chr2:174096400-174107000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr2:174096400-174109200	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr2:174096400-174112600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:174096600-174099600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr2:174096600-174099600	Strong transcription	A549	lung
31	chr2:174096600-174103400	Weak transcription	Duodenum Mucosa	Duodenum
32	chr2:174096600-174104400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr2:174096600-174105600	Strong transcription	Stomach Smooth Muscle	stomach
34	chr2:174096600-174110800	Weak transcription	Small Intestine	intestine
35	chr2:174096600-174128800	Weak transcription	Pancreas	Pancrea
36	chr2:174096600-174130800	Weak transcription	Gastric	stomach
37	chr2:174096800-174099600	Strong transcription	Placenta	Placenta
38	chr2:174096800-174102800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:174096800-174108200	Weak transcription	Fetal Heart	heart
40	chr2:174096800-174108400	Strong transcription	Adipose Nuclei	Adipose
41	chr2:174097000-174100000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr2:174097000-174100800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:174097000-174101200	Strong transcription	Fetal Intestine Large	intestine
44	chr2:174097000-174102000	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr2:174097400-174099600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:174097400-174100000	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr2:174097600-174099600	Strong transcription	Liver	Liver
48	chr2:174097600-174099600	Strong transcription	Left Ventricle	heart
49	chr2:174097600-174099800	Strong transcription	Colon Smooth Muscle	Colon
50	chr2:174097600-174100200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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