Variant report

Variant	rs72884382
Chromosome Location	chr4:98053027-98053028
allele	G/T
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:13)

rs_ID	r²[population]
rs6822376	1.00[AMR][1000 genomes]
rs72880581	0.83[AFR][1000 genomes]
rs72880583	0.88[AFR][1000 genomes]
rs72884323	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72884325	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72884348	1.00[AMR][1000 genomes]
rs72884351	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72884363	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72884372	1.00[AMR][1000 genomes]
rs72884375	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72884377	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7690146	1.00[AMR][1000 genomes]
rs7690871	0.98[AFR][1000 genomes];1.00[AMR][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	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1002766	chr4:98006688-98128416	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv537192	chr4:98006688-98128416	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3370026	chr4:98044823-98067071	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98051600-98055600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr4:98052600-98053400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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