Variant report

Variant	rs10266009
Chromosome Location	chr7:26411087-26411088
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10265225	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34311960	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34772540	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3801877	1.00[ASN][1000 genomes]
rs71521763	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7801652	1.00[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	nsv1021308	chr7:26116605-26419720	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv1029596	chr7:26302739-26737913	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv538804	chr7:26302739-26737913	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26375000-26414000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:26385600-26414200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:26389000-26413200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:26398600-26415400	Weak transcription	HMEC	breast
5	chr7:26402600-26415200	Enhancers	Liver	Liver
6	chr7:26403800-26415600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:26404800-26411200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr7:26404800-26414000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:26404800-26415200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr7:26405200-26413800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr7:26405200-26414000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:26405400-26413800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr7:26405400-26414600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr7:26405800-26414600	Weak transcription	K562	blood
15	chr7:26407000-26411200	Weak transcription	Fetal Intestine Small	intestine
16	chr7:26407400-26411800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr7:26407400-26412000	Weak transcription	Placenta	Placenta
18	chr7:26407400-26415400	Weak transcription	HepG2	liver
19	chr7:26407400-26415600	Weak transcription	Spleen	Spleen
20	chr7:26407600-26413800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr7:26407600-26415400	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr7:26409600-26413800	Weak transcription	Fetal Brain Male	brain
23	chr7:26409800-26412000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr7:26409800-26413600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr7:26409800-26415400	Weak transcription	GM12878-XiMat	blood
26	chr7:26410000-26411800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr7:26410000-26413000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr7:26410200-26411200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:26410200-26411800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:26410200-26412200	Weak transcription	Fetal Intestine Large	intestine
31	chr7:26410200-26412200	Enhancers	HUVEC	blood vessel
32	chr7:26410200-26412400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:26410200-26413200	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr7:26410200-26413400	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr7:26410200-26413800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr7:26410200-26414800	Weak transcription	Primary T cells from cord blood	blood
37	chr7:26410200-26414800	Weak transcription	Fetal Thymus	thymus
38	chr7:26410200-26415200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:26410200-26415400	Weak transcription	Adipose Nuclei	Adipose
40	chr7:26410400-26411200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:26410400-26411400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr7:26410400-26413200	Strong transcription	Primary B cells from cord blood	blood
43	chr7:26410600-26411200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr7:26410600-26414600	Strong transcription	Primary neutrophils fromperipheralblood	blood
45	chr7:26410800-26412000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:26411000-26414400	Strong transcription	Primary B cells from peripheral blood	blood

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