Variant report

Variant	rs7802675
Chromosome Location	chr7:137327170-137327171
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	chr7:137326769..137328624-chr7:137333042..137335540,3	K562	blood:
2	chr7:137327026..137328624-chr7:137333042..137335182,2	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10429242	1.00[AMR][1000 genomes]
rs1609249	1.00[AMR][1000 genomes]
rs56757293	1.00[AMR][1000 genomes]
rs57437520	1.00[AMR][1000 genomes]
rs58529038	1.00[AMR][1000 genomes]
rs58688605	1.00[AMR][1000 genomes]
rs61051125	1.00[AMR][1000 genomes]
rs6958415	1.00[AMR][1000 genomes]
rs6967718	1.00[AMR][1000 genomes]
rs706571	1.00[AMR][1000 genomes]
rs7779815	1.00[YRI][hapmap]
rs7808760	1.00[AMR][1000 genomes]
rs834449	1.00[AMR][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	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1022793	chr7:137187383-137619359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	esv1812888	chr7:137283212-137366467	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137282800-137337400	Weak transcription	HSMMtube	muscle
2	chr7:137294000-137328400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr7:137313200-137328400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr7:137320200-137352600	Weak transcription	Aorta	Aorta
5	chr7:137320400-137328400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:137321400-137337000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:137325800-137337400	Weak transcription	HSMM	muscle
8	chr7:137326800-137327200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:137326800-137327200	Genic enhancers	Muscle Satellite Cultured Cells	--
10	chr7:137326800-137327200	Enhancers	NHLF	lung
11	chr7:137326800-137327200	Genic enhancers	Osteobl	bone
12	chr7:137326800-137327400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr7:137326800-137327800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr7:137326800-137327800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:137327000-137327400	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:137327000-137327400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr7:137327000-137327400	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr7:137327000-137327600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:137327000-137327600	Enhancers	Colon Smooth Muscle	Colon
20	chr7:137327000-137327600	Enhancers	Hela-S3	cervix
21	chr7:137327000-137327600	Enhancers	NHDF-Ad	bronchial
22	chr7:137327000-137328200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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