Variant report

Variant	rs73928943
Chromosome Location	chr2:33845815-33845816
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17013659	0.90[AMR][1000 genomes]
rs17657503	1.00[AMR][1000 genomes]
rs55732959	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57979664	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59455759	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73926695	1.00[AMR][1000 genomes]
rs73928936	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73928940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73928945	1.00[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33825200-33846600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr2:33834200-33846600	Weak transcription	Psoas Muscle	Psoas
3	chr2:33844400-33848200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr2:33845200-33846200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr2:33845200-33859400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:33845200-33859600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:33845600-33849400	Weak transcription	iPS DF 6.9 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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