Variant report

Variant	rs74098707
Chromosome Location	chr1:85365947-85365948
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs17117109	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28524614	0.87[AMR][1000 genomes]
rs55768845	1.00[AMR][1000 genomes]
rs55837625	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55965798	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56822129	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58206393	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59309353	1.00[EUR][1000 genomes]
rs59651987	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59717651	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59811689	1.00[AMR][1000 genomes]
rs59843423	0.87[AMR][1000 genomes]
rs60736067	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60739573	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61296345	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61506051	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6693142	1.00[EUR][1000 genomes]
rs74096200	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74098703	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7544744	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7547127	0.87[AMR][1000 genomes]
rs7553171	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830448	chr1:85294094-85491110	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv470724	chr1:85334788-85585260	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv462383	chr1:85334788-85594466	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv546700	chr1:85334788-85594466	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv947434	chr1:85334915-85594135	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85360200-85382600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:85365800-85366200	Enhancers	Fetal Lung	lung

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