Variant report

Variant	rs73114982
Chromosome Location	chr12:56024124-56024125
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs17117846	0.92[ASN][1000 genomes]
rs17511746	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4759006	0.86[ASN][1000 genomes]
rs55819151	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs55847809	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs56243753	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs56315406	0.89[ASN][1000 genomes]
rs56377768	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61746285	0.89[ASN][1000 genomes]
rs66592094	0.92[ASN][1000 genomes]
rs73114979	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73114980	0.96[ASN][1000 genomes]
rs73117220	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73117228	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73117233	0.82[AMR][1000 genomes];0.92[ASN][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	nsv559001	chr12:55507465-56057708	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv948625	chr12:55838718-56118833	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56017000-56026000	Weak transcription	Right Atrium	heart
2	chr12:56018800-56025000	Weak transcription	Left Ventricle	heart
3	chr12:56020600-56025200	Weak transcription	Right Ventricle	heart
4	chr12:56022800-56024400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr12:56023000-56025400	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr12:56023200-56036800	Weak transcription	Spleen	Spleen
7	chr12:56023800-56025400	Weak transcription	Monocytes-CD14+_RO01746	blood

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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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