Variant report

Variant	rs73955268
Chromosome Location	chr18:30308003-30308004
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13339718	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963740	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16963802	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28435690	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28448643	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28564043	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs689524	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7230398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7231950	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7235638	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7238067	1.00[ASN][1000 genomes]
rs73955260	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8085109	1.00[ASN][1000 genomes]
rs8089631	1.00[EUR][1000 genomes]
rs9950337	1.00[EUR][1000 genomes]
rs9951832	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9958052	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30305600-30310000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr18:30305800-30308400	Weak transcription	Primary B cells from cord blood	blood
3	chr18:30307000-30309600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:30307200-30308400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr18:30307200-30310000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr18:30307800-30308200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr18:30307800-30308400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr18:30307800-30309400	Strong transcription	HepG2	liver

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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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