Variant report

Variant	rs7858926
Chromosome Location	chr9:101131753-101131754
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10122333	0.87[AFR][1000 genomes]
rs7031028	0.87[YRI][hapmap]
rs7860916	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7871107	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101120600-101134400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr9:101126600-101142600	Weak transcription	Brain Angular Gyrus	brain
3	chr9:101127800-101134200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr9:101128200-101164200	Weak transcription	Brain Germinal Matrix	brain
5	chr9:101129000-101156000	Weak transcription	Fetal Brain Female	brain
6	chr9:101130400-101134800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr9:101130800-101135600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr9:101131200-101132000	Enhancers	K562	blood
9	chr9:101131200-101135600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:101131400-101132600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr9:101131400-101135200	Weak transcription	Osteobl	bone
12	chr9:101131400-101135400	Weak transcription	NH-A	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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