Variant report

Variant	rs73391588
Chromosome Location	chr7:85150861-85150862
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs59194733	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73391537	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73391556	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73391566	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73391570	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73391599	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73393509	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73393514	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916645	chr7:84678606-85420011	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv869255	chr7:84678606-85444155	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv3327487	chr7:84901505-85320690	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv888649	chr7:85099898-85356773	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2761345	chr7:85104681-85187726	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1034789	chr7:85137730-85175007	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv888650	chr7:85138665-85267174	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1021810	chr7:85148963-85194663	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 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	chr7:85150400-85151000	Enhancers	Colon Smooth Muscle	Colon
2	chr7:85150400-85151000	Enhancers	Fetal Stomach	stomach
3	chr7:85150400-85151000	Enhancers	NHLF	lung
4	chr7:85150600-85151000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:85150600-85151000	Enhancers	Fetal Heart	heart
6	chr7:85150800-85151000	Enhancers	Fetal Kidney	kidney
7	chr7:85150800-85151000	Enhancers	Fetal Lung	lung
8	chr7:85150800-85151000	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr7:85150800-85151200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:85150800-85151200	Enhancers	Small Intestine	intestine

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

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