Variant report

Variant	rs73918091
Chromosome Location	chr2:21276956-21276957
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12720761	1.00[AMR][1000 genomes]
rs55899854	1.00[AMR][1000 genomes]
rs56300790	1.00[AMR][1000 genomes]
rs56362198	1.00[AMR][1000 genomes]
rs56370608	1.00[AMR][1000 genomes]
rs57300286	1.00[AMR][1000 genomes]
rs58233853	1.00[AMR][1000 genomes]
rs58480104	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59771269	1.00[AMR][1000 genomes]
rs59952985	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73918012	1.00[AMR][1000 genomes]
rs73918094	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73918095	1.00[AMR][1000 genomes]
rs73918098	1.00[AMR][1000 genomes]
rs73918099	1.00[AMR][1000 genomes]
rs73918100	1.00[AMR][1000 genomes]
rs73918101	1.00[AMR][1000 genomes]
rs73918102	1.00[AMR][1000 genomes]
rs73919803	1.00[AMR][1000 genomes]
rs73919804	1.00[AMR][1000 genomes]
rs73919805	1.00[AMR][1000 genomes]
rs73919806	1.00[AMR][1000 genomes]
rs73919807	1.00[AMR][1000 genomes]
rs73919810	1.00[AMR][1000 genomes]
rs73920458	1.00[AMR][1000 genomes]
rs73921327	0.80[AFR][1000 genomes];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	nsv873728	chr2:21250914-21460786	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21271200-21279000	Weak transcription	Fetal Intestine Small	intestine
2	chr2:21274400-21278800	Enhancers	HepG2	liver
3	chr2:21275600-21278200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:21276800-21277400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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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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