Variant report

Variant	rs73891033
Chromosome Location	chr3:191390335-191390336
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10937508	0.91[AFR][1000 genomes]
rs10937509	0.91[AFR][1000 genomes]
rs55844081	0.91[AFR][1000 genomes]
rs57326138	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57479631	0.91[AFR][1000 genomes]
rs57757618	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58464844	0.91[AFR][1000 genomes]
rs60279150	1.00[AFR][1000 genomes]
rs60612838	0.91[AFR][1000 genomes]
rs61198908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61497004	0.91[AFR][1000 genomes]
rs73888408	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73888410	0.91[AFR][1000 genomes]
rs73888411	0.91[AFR][1000 genomes]
rs73888412	1.00[AFR][1000 genomes]
rs73888414	1.00[AFR][1000 genomes]
rs73888415	0.91[AFR][1000 genomes]
rs73888416	1.00[AFR][1000 genomes]
rs73888417	0.91[AFR][1000 genomes]
rs73888418	0.91[AFR][1000 genomes]
rs73888419	0.91[AFR][1000 genomes]
rs73888420	0.91[AFR][1000 genomes]
rs73888421	0.91[AFR][1000 genomes]
rs73888422	0.91[AFR][1000 genomes]
rs73891036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915689	chr3:191244719-191479974	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv997817	chr3:191284834-191475809	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1001082	chr3:191320636-191579587	Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1009378	chr3:191359361-191928703	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1000060	chr3:191359361-191935048	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv437360	chr3:191371101-191392897	Genic enhancers Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1002406	chr3:191380544-191404841	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191389600-191390800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr3:191390000-191391000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr3:191390200-191390600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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