Variant report

Variant	rs73726735
Chromosome Location	chr7:136278527-136278528
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1425154	1.00[AMR][1000 genomes]
rs56877552	1.00[AMR][1000 genomes]
rs57349342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73726151	1.00[AMR][1000 genomes]
rs73726734	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518439	chr7:136134265-136452082	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136276400-136279000	Weak transcription	Fetal Stomach	stomach
2	chr7:136276600-136279200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr7:136278200-136278600	Weak transcription	Colon Smooth Muscle	Colon

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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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