Variant report

Variant	rs7799667
Chromosome Location	chr7:128976323-128976324
allele	A/T
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:5)

rs_ID	r²[population]
rs73465341	0.80[AFR][1000 genomes]
rs73465351	0.80[AFR][1000 genomes]
rs73470399	0.93[AFR][1000 genomes]
rs73472326	1.00[AFR][1000 genomes]
rs73477662	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525482	chr7:128890812-129045191	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv516498	chr7:128901429-129072024	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	esv3331483	chr7:128918442-129082887	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv428508	chr7:128946738-129114691	Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128956000-128977400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr7:128958000-128981000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:128964200-128981000	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr7:128964600-128981000	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr7:128964800-128976400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:128965200-128984200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr7:128965400-128994600	Weak transcription	Primary B cells from cord blood	blood
8	chr7:128965600-128978200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:128965800-128980800	Weak transcription	Fetal Intestine Small	intestine
10	chr7:128965800-128995800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr7:128972600-128981200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:128972800-128978800	Weak transcription	HMEC	breast
13	chr7:128972800-128984000	Weak transcription	HSMMtube	muscle
14	chr7:128972800-128984200	Weak transcription	HSMM	muscle
15	chr7:128973200-128984000	Weak transcription	NHEK	skin
16	chr7:128973400-128991000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:128973600-128982800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr7:128975000-129002600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr7:128975800-128978000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:128975800-128980800	Weak transcription	Primary T cells from cord blood	blood

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