Variant report

Variant	rs74090903
Chromosome Location	chr12:48888744-48888745
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11168585	1.00[AMR][1000 genomes]
rs12306781	1.00[AMR][1000 genomes]
rs2705132	0.83[AMR][1000 genomes]
rs57214338	1.00[AMR][1000 genomes]
rs57847713	1.00[AMR][1000 genomes]
rs58537022	1.00[AMR][1000 genomes]
rs59814472	1.00[AMR][1000 genomes]
rs60157593	1.00[AMR][1000 genomes]
rs60457957	1.00[AMR][1000 genomes]
rs73296803	1.00[AMR][1000 genomes]
rs73296804	1.00[AMR][1000 genomes]
rs73296814	1.00[AMR][1000 genomes]
rs73296825	1.00[AMR][1000 genomes]
rs73296837	1.00[AMR][1000 genomes]
rs73298787	1.00[AMR][1000 genomes]
rs73298791	1.00[AMR][1000 genomes]
rs73298792	1.00[AMR][1000 genomes]
rs74090293	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	nsv427911	chr12:48670336-48979396	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
2	nsv975416	chr12:48882416-48893049	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr12:48887000-48891800	Weak transcription	Brain Hippocampus Middle	brain
2	chr12:48887600-48890000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr12:48888600-48888800	ZNF genes & repeats	Spleen	Spleen

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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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