Variant report

Variant	rs73835900
Chromosome Location	chr3:69610444-69610445
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs17006070	1.00[AMR][1000 genomes]
rs17006073	1.00[AMR][1000 genomes]
rs17006111	1.00[AMR][1000 genomes]
rs55690669	1.00[AMR][1000 genomes]
rs55746200	1.00[AMR][1000 genomes]
rs73835877	1.00[AMR][1000 genomes]
rs73836165	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007730	chr3:69355932-69730587	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3426797	chr3:69433086-69777229	Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1004470	chr3:69597148-69728231	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69604400-69612400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:69604400-69615200	Weak transcription	Spleen	Spleen
3	chr3:69607400-69611400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr3:69608200-69610600	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr3:69608400-69615400	Weak transcription	Right Ventricle	heart
6	chr3:69608600-69611400	Weak transcription	Brain Angular Gyrus	brain
7	chr3:69608800-69611200	Weak transcription	Brain Anterior Caudate	brain
8	chr3:69608800-69615200	Weak transcription	Right Atrium	heart
9	chr3:69609800-69610600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr3:69610000-69612800	Enhancers	Fetal Lung	lung
11	chr3:69610400-69610600	Enhancers	Brain Cingulate Gyrus	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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