Variant report

Variant	rs73480179
Chromosome Location	chr6:81633924-81633925
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs6940338	1.00[AMR][1000 genomes]
rs73463306	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73463330	1.00[AMR][1000 genomes]
rs73463349	1.00[AMR][1000 genomes]
rs73463361	1.00[AMR][1000 genomes]
rs73463382	1.00[AMR][1000 genomes]
rs73465305	1.00[AMR][1000 genomes]
rs73474836	1.00[AMR][1000 genomes]
rs73476343	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73476353	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478111	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478117	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478119	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73482319	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73482322	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531333	chr6:81042427-81836484	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv886315	chr6:81352515-81946866	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv886318	chr6:81447367-81769538	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2763957	chr6:81567637-81656379	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1032130	chr6:81572030-81722231	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2762604	chr6:81593275-81742093	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv428487	chr6:81607405-81742838	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv830709	chr6:81615127-81793247	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv508418	chr6:81616151-81638965	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81632800-81634200	Enhancers	Rectal Smooth Muscle	rectum
2	chr6:81633000-81634800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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