Variant report

Variant	rs72953558
Chromosome Location	chr1:86993529-86993530
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs72951876	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	nsv1003838	chr1:86591841-87212231	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86992600-86993800	Enhancers	Fetal Intestine Large	intestine
2	chr1:86992600-86993800	Enhancers	Fetal Intestine Small	intestine
3	chr1:86992600-86993800	Enhancers	HUVEC	blood vessel
4	chr1:86992800-86993800	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr1:86993200-86993600	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr1:86993200-86993600	Enhancers	Stomach Mucosa	stomach
7	chr1:86993400-86993600	Flanking Active TSS	Duodenum Mucosa	Duodenum

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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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