Variant report

Variant	rs73091021
Chromosome Location	chr1:212081482-212081483
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10494945	1.00[AMR][1000 genomes]
rs10494946	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1343736	0.83[AMR][1000 genomes]
rs17018161	1.00[AMR][1000 genomes]
rs17018191	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17042028	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56945865	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57554409	0.83[AMR][1000 genomes]
rs60083191	1.00[AMR][1000 genomes]
rs61511331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73091010	1.00[AMR][1000 genomes]
rs73091020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73091023	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73091026	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73091029	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73091032	0.92[AFR][1000 genomes]
rs73091035	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762218	chr1:212046447-212087682	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
2	esv3527308	chr1:212079479-212082377	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
3	esv3452684	chr1:212080132-212081517	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212076200-212083600	Weak transcription	Pancreas	Pancrea
2	chr1:212077200-212082600	Weak transcription	Colonic Mucosa	Colon
3	chr1:212077400-212082400	Weak transcription	Adipose Nuclei	Adipose
4	chr1:212078000-212082400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr1:212078000-212082400	Weak transcription	HepG2	liver
6	chr1:212078400-212081800	Weak transcription	Liver	Liver
7	chr1:212079600-212087400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:212080400-212087600	Enhancers	Fetal Intestine Large	intestine
9	chr1:212080800-212087000	Enhancers	Fetal Intestine Small	intestine
10	chr1:212081000-212085000	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr1:212081200-212082200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr1:212081200-212083600	Weak transcription	Esophagus	oesophagus
13	chr1:212081400-212081600	Flanking Active TSS	GM12878-XiMat	blood

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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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