Variant report

Variant	rs372032635
Chromosome Location	chr8:89013882-89013883
allele	G/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	nsv1029898	chr8:88837956-89606641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv428520	chr8:88933423-89089323	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	esv2758163	chr8:88963829-89133704	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	esv2759625	chr8:88963829-89133704	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	esv2762758	chr8:89013301-89033922	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89012200-89014800	Enhancers	Primary hematopoietic stem cells	blood
2	chr8:89012800-89014800	Enhancers	Primary B cells from peripheral blood	blood
3	chr8:89013000-89014000	Enhancers	Fetal Kidney	kidney
4	chr8:89013200-89014000	Flanking Active TSS	Primary B cells from cord blood	blood
5	chr8:89013400-89014200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:89013400-89014800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr8:89013400-89014800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr8:89013400-89017200	Weak transcription	Aorta	Aorta
9	chr8:89013600-89014000	Enhancers	Brain Hippocampus Middle	brain
10	chr8:89013600-89014000	Enhancers	Brain Substantia Nigra	brain
11	chr8:89013600-89014000	Enhancers	Osteobl	bone
12	chr8:89013600-89014200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr8:89013600-89015000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:89013600-89018800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr8:89013800-89014600	Enhancers	HUVEC	blood vessel
16	chr8:89013800-89014800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr8:89013800-89018800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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