Variant report

Variant	rs569769670
Chromosome Location	chr7:26745326-26745327
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv830929	chr7:26587888-26749735	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv5672	chr7:26711462-26757891	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1018125	chr7:26745074-26789814	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26705000-26759600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr7:26729000-26756400	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:26729200-26747000	Weak transcription	Primary B cells from cord blood	blood
4	chr7:26729200-26747000	Weak transcription	Primary B cells from peripheral blood	blood
5	chr7:26729600-26750000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:26730000-26747000	Weak transcription	Fetal Kidney	kidney
7	chr7:26731800-26779200	Weak transcription	Spleen	Spleen
8	chr7:26732200-26765000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr7:26740400-26782400	Weak transcription	Fetal Intestine Small	intestine
10	chr7:26740600-26745400	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr7:26742800-26750800	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr7:26743400-26745400	Enhancers	Adipose Nuclei	Adipose
13	chr7:26743800-26745600	Enhancers	Colon Smooth Muscle	Colon
14	chr7:26743800-26745600	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr7:26743800-26746400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:26743800-26746400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr7:26743800-26747800	Enhancers	NHDF-Ad	bronchial
18	chr7:26743800-26747800	Enhancers	NHLF	lung
19	chr7:26744000-26746000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:26744000-26746200	Enhancers	Stomach Smooth Muscle	stomach
21	chr7:26744200-26746000	Enhancers	Rectal Smooth Muscle	rectum
22	chr7:26744200-26746200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:26744200-26747600	Enhancers	HUVEC	blood vessel
24	chr7:26744400-26745400	Enhancers	Fetal Muscle Leg	muscle
25	chr7:26744400-26745800	Enhancers	HSMMtube	muscle
26	chr7:26744400-26745800	Enhancers	NH-A	brain
27	chr7:26744400-26746000	Enhancers	HSMM	muscle
28	chr7:26744400-26746200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:26744400-26746400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:26744600-26745800	Enhancers	Primary hematopoietic stem cells	blood
31	chr7:26745000-26745800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:26745000-26745800	Enhancers	HMEC	breast
33	chr7:26745000-26745800	Enhancers	NHEK	skin
34	chr7:26745000-26780800	Weak transcription	Aorta	Aorta
35	chr7:26745200-26745600	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr7:26745200-26745600	Flanking Active TSS	A549	lung
37	chr7:26745200-26745600	Enhancers	HepG2	liver
38	chr7:26745200-26746000	Enhancers	Osteobl	bone
39	chr7:26745200-26746200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:26745200-26747200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:26745200-26747200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:26745200-26750200	Weak transcription	Fetal Lung	lung

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