Variant report

Variant	rs7901722
Chromosome Location	chr10:61530612-61530613
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10821593	0.93[EUR][1000 genomes]
rs10994004	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10994005	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11817729	0.92[EUR][1000 genomes]
rs12242758	0.94[EUR][1000 genomes]
rs12243559	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12267686	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16914091	0.86[ASN][1000 genomes]
rs16914097	0.86[ASN][1000 genomes]
rs1949257	0.94[EUR][1000 genomes]
rs55958518	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56692362	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7901952	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs882896	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61530600-61530800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
2	chr10:61530600-61530800	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr10:61530600-61532000	Enhancers	Rectal Mucosa Donor 29	rectum

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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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