Variant report

Variant	rs73772925
Chromosome Location	chr5:93041713-93041714
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17083311	1.00[AMR][1000 genomes]
rs17083335	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58553637	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59348704	1.00[AMR][1000 genomes]
rs6875129	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6878031	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6897186	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73772929	1.00[AMR][1000 genomes]
rs73772931	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73773533	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	nsv830404	chr5:92868336-93048257	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv532196	chr5:92933949-93573527	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:93003200-93044400	Weak transcription	Primary B cells from cord blood	blood
2	chr5:93035600-93044200	Weak transcription	Psoas Muscle	Psoas
3	chr5:93038400-93076200	Weak transcription	Ovary	ovary
4	chr5:93038800-93050400	Weak transcription	Fetal Intestine Small	intestine
5	chr5:93040000-93048600	Weak transcription	Primary T cells from cord blood	blood
6	chr5:93040600-93042600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr5:93040600-93088600	Weak transcription	Aorta	Aorta
8	chr5:93040800-93042800	Enhancers	NHLF	lung
9	chr5:93041000-93051400	Weak transcription	Fetal Heart	heart
10	chr5:93041400-93042200	Weak transcription	Fetal Brain Male	brain
11	chr5:93041400-93042200	Enhancers	NH-A	brain
12	chr5:93041400-93042200	Enhancers	Osteobl	bone
13	chr5:93041400-93042400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr5:93041600-93042200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:93041600-93042200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:93041600-93042400	Enhancers	NHDF-Ad	bronchial

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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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