Variant report

Variant	rs17160998
Chromosome Location	chr7:86416805-86416806
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1013011	0.95[YRI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs17161001	0.95[YRI][hapmap];0.81[AFR][1000 genomes]
rs17161004	0.95[YRI][hapmap];0.81[AFR][1000 genomes]
rs17161007	0.95[YRI][hapmap];0.81[AFR][1000 genomes]
rs17161014	0.81[AFR][1000 genomes]
rs17161023	0.95[YRI][hapmap];0.81[AFR][1000 genomes]
rs17697543	0.84[AFR][1000 genomes]
rs2188291	0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2214010	0.91[YRI][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2214011	0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs2214859	0.81[AFR][1000 genomes]
rs3922329	0.95[YRI][hapmap]
rs60525216	0.81[AFR][1000 genomes]
rs7776998	0.95[YRI][hapmap];0.80[AFR][1000 genomes]

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	nsv1025032	chr7:86032479-86642973	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv831053	chr7:86268171-86440999	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1025277	chr7:86299224-87206007	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
4	nsv538999	chr7:86299224-87206007	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
5	nsv532147	chr7:86299225-87121975	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86415600-86417000	Strong transcription	Brain Hippocampus Middle	brain
2	chr7:86415600-86418000	Enhancers	GM12878-XiMat	blood
3	chr7:86415800-86419400	Weak transcription	Brain Angular Gyrus	brain
4	chr7:86416200-86419200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr7:86416400-86419000	Weak transcription	Fetal Brain Male	brain
6	chr7:86416600-86417400	Enhancers	Brain Anterior Caudate	brain
7	chr7:86416600-86418200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr7:86416600-86426200	Weak transcription	Fetal Brain Female	brain
9	chr7:86416800-86418200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:86416800-86418400	Weak transcription	Brain Germinal Matrix	brain
11	chr7:86416800-86418400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr7:86416800-86419000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:86416800-86420800	Weak transcription	Brain Substantia Nigra	brain
14	chr7:86416800-86421200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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