Variant report

Variant	rs12347800
Chromosome Location	chr9:72416541-72416542
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10217593	0.86[AFR][1000 genomes]
rs10283869	1.00[AMR][1000 genomes]
rs12340071	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12342754	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12343258	0.91[AFR][1000 genomes]
rs12344521	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12345510	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12349363	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28498152	1.00[AMR][1000 genomes]
rs28731505	1.00[AMR][1000 genomes]
rs7036155	1.00[AMR][1000 genomes]
rs7854014	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050920	chr9:72345297-72579301	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv831611	chr9:72361905-72512134	Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv893438	chr9:72363992-72720438	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72414000-72416800	Weak transcription	HepG2	liver
2	chr9:72414000-72417000	Weak transcription	K562	blood
3	chr9:72414000-72418000	Weak transcription	Fetal Lung	lung

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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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