Variant report

Variant	rs57133697
Chromosome Location	chr2:21221882-21221883
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12691188	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12992267	0.93[AFR][1000 genomes]
rs1801702	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34776010	0.93[AFR][1000 genomes]
rs497166	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55907101	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72654432	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs952274	0.93[AFR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21216400-21225600	Weak transcription	Aorta	Aorta
2	chr2:21220200-21225600	Weak transcription	Left Ventricle	heart
3	chr2:21220600-21224200	Weak transcription	HepG2	liver
4	chr2:21221000-21224400	Weak transcription	Fetal Intestine Small	intestine
5	chr2:21221600-21223200	Weak transcription	Liver	Liver
6	chr2:21221800-21224800	Weak transcription	Fetal Intestine Large	intestine

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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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