Variant report

Variant	rs16917111
Chromosome Location	chr9:101321063-101321064
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10521035	1.00[CEU][hapmap]
rs10986439	1.00[CEU][hapmap]
rs12340370	1.00[CHB][hapmap]
rs16916050	1.00[CEU][hapmap]
rs4743219	1.00[JPT][hapmap]
rs59391327	0.85[EUR][1000 genomes]
rs7023937	1.00[CEU][hapmap]
rs73488496	1.00[EUR][1000 genomes]
rs957339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	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	nsv831665	chr9:101170061-101367692	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv614936	chr9:101182698-101680380	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv6633	chr9:101308371-101342811	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101314400-101326400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:101320400-101321400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr9:101320400-101321400	Enhancers	Brain Hippocampus Middle	brain
4	chr9:101320400-101322400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:101320400-101322600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr9:101320600-101321200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr9:101320600-101321200	Enhancers	Osteobl	bone
8	chr9:101320600-101322200	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr9:101320800-101321200	Enhancers	Brain Cingulate Gyrus	brain
10	chr9:101320800-101321200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr9:101320800-101321200	Enhancers	GM12878-XiMat	blood
12	chr9:101320800-101321200	Enhancers	K562	blood
13	chr9:101320800-101321200	Enhancers	NH-A	brain
14	chr9:101320800-101322400	Enhancers	Liver	Liver
15	chr9:101321000-101321200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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