Variant report

Variant	rs73502498
Chromosome Location	chr11:75442755-75442756
allele	C/T
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:4)

rs_ID	r²[population]
rs12276456	1.00[EUR][1000 genomes]
rs12279237	1.00[EUR][1000 genomes]
rs12284314	1.00[EUR][1000 genomes]
rs73502496	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3381903	chr11:75123498-75587233	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
2	nsv897924	chr11:75424546-75678647	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75433200-75443200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:75435200-75443200	Strong transcription	Rectal Mucosa Donor 31	rectum
3	chr11:75435600-75443000	Strong transcription	Fetal Intestine Large	intestine
4	chr11:75436800-75443000	Strong transcription	Fetal Intestine Small	intestine
5	chr11:75437400-75444000	Weak transcription	Right Ventricle	heart
6	chr11:75437400-75444400	Weak transcription	Right Atrium	heart
7	chr11:75437600-75444400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr11:75438000-75442800	Strong transcription	Liver	Liver
9	chr11:75440200-75444200	Weak transcription	Adipose Nuclei	Adipose
10	chr11:75440400-75444200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr11:75442200-75443200	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr11:75442200-75443600	Strong transcription	Colonic Mucosa	Colon
13	chr11:75442400-75444000	Genic enhancers	Duodenum Mucosa	Duodenum
14	chr11:75442600-75444200	Weak transcription	HepG2	liver

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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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