Variant report

Variant	rs73692600
Chromosome Location	chr8:91604454-91604455
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10046720	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10087211	0.81[AMR][1000 genomes]
rs10094321	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10098293	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10098726	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10113048	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs16904906	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs16904915	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs16905034	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs16905035	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs16905036	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs28489185	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs28495879	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs28552751	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs28557468	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs56021347	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs56187777	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs73692314	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs73692316	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs73692470	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs73692595	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs73692598	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9297873	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9297878	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91594600-91621600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:91597600-91606400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:91597800-91605800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:91603200-91605400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:91603200-91605600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr8:91603600-91605000	Weak transcription	ES-WA7 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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