Variant report

Variant	rs35092707
Chromosome Location	chr5:68187114-68187115
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs34044149	0.87[AMR][1000 genomes]
rs34264944	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs34845252	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35260480	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs35428898	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35666670	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6891704	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6891706	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs71622264	0.95[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7730743	0.87[AMR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68179600-68195200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr5:68180200-68190400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr5:68180600-68187200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr5:68184000-68187200	Weak transcription	Fetal Thymus	thymus
5	chr5:68187000-68188600	Enhancers	Primary T cells from cord blood	blood

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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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