Variant report

Variant	rs719144
Chromosome Location	chr6:82331788-82331789
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10806229	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11752435	0.83[EUR][1000 genomes]
rs1341220	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13437553	0.83[ASW][hapmap];0.87[CHD][hapmap];0.83[TSI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1917063	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4324818	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6454229	0.81[AMR][1000 genomes]
rs6454237	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7763102	0.81[AMR][1000 genomes]
rs7771821	0.81[AMR][1000 genomes]
rs9294235	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9341895	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9344208	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9344211	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9344214	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9344215	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9361840	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9361847	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9449361	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82318000-82356600	Weak transcription	Aorta	Aorta
2	chr6:82329600-82332200	Weak transcription	Placenta	Placenta
3	chr6:82331600-82332000	Enhancers	Osteobl	bone
4	chr6:82331600-82332400	Enhancers	NHDF-Ad	bronchial

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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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