Variant report

Variant	rs12646006
Chromosome Location	chr4:62615182-62615183
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10013153	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11732258	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12646895	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13132632	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13138257	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2343575	0.88[EUR][1000 genomes]
rs2343576	0.82[EUR][1000 genomes]
rs2343577	0.82[EUR][1000 genomes]
rs2343578	0.83[EUR][1000 genomes]
rs2343579	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2343580	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4241640	0.83[EUR][1000 genomes]
rs4339245	0.82[EUR][1000 genomes]
rs4371644	0.83[EUR][1000 genomes]
rs4458480	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4495065	0.82[EUR][1000 genomes]
rs4513598	0.91[EUR][1000 genomes]
rs4639106	0.83[EUR][1000 genomes]
rs4860100	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4860102	0.81[AMR][1000 genomes]
rs62306769	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6551648	0.85[EUR][1000 genomes]
rs6551649	0.82[EUR][1000 genomes]
rs6551654	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6848543	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7376314	0.82[EUR][1000 genomes]
rs7663116	0.86[EUR][1000 genomes]
rs7684797	0.85[EUR][1000 genomes]
rs7691558	0.86[EUR][1000 genomes]
rs7691739	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7691805	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7695664	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7699021	0.86[EUR][1000 genomes]
rs7699533	0.85[EUR][1000 genomes]
rs9998958	0.80[AMR][1000 genomes];0.84[EUR][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	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62609600-62616600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:62610200-62615600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:62610200-62616600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:62610400-62615200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:62610400-62616600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:62610400-62625400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:62611000-62615400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:62611000-62616400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr4:62611800-62615400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr4:62613600-62615600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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