Variant report

Variant	rs73752801
Chromosome Location	chr5:50243920-50243921
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10054384	0.89[ASN][1000 genomes]
rs16887696	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs16888239	0.89[ASN][1000 genomes]
rs185137	0.89[ASN][1000 genomes]
rs250233	0.89[ASN][1000 genomes]
rs250236	0.89[ASN][1000 genomes]
rs250237	0.89[ASN][1000 genomes]
rs4626298	0.89[ASN][1000 genomes]
rs5005508	0.89[ASN][1000 genomes]
rs55753044	0.87[AFR][1000 genomes]
rs55833214	0.89[ASN][1000 genomes]
rs6864779	0.89[ASN][1000 genomes]
rs72758259	0.89[ASN][1000 genomes]
rs72758263	0.89[ASN][1000 genomes]
rs72758266	0.89[ASN][1000 genomes]
rs73752784	0.80[AFR][1000 genomes]
rs7703469	0.89[ASN][1000 genomes]
rs7717928	0.89[ASN][1000 genomes]
rs7725532	0.89[ASN][1000 genomes]
rs7730386	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034445	chr5:49986171-50492609	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv598116	chr5:50064292-50318550	Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv830286	chr5:50165805-50374600	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv511286	chr5:50231548-50254200	Enhancers	TF binding region Chromatin interactive region	2 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	chr5:50243600-50244000	Enhancers	Fetal Brain Female	brain
2	chr5:50243600-50244200	Enhancers	Fetal Heart	heart
3	chr5:50243800-50244400	Enhancers	Stomach Smooth Muscle	stomach

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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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