Variant report

Variant	rs4535596
Chromosome Location	chr6:82720589-82720590
allele	A/C
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]
rs10755418	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10943842	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10943845	0.82[EUR][1000 genomes]
rs12194197	0.89[EUR][1000 genomes]
rs12199519	0.89[EUR][1000 genomes]
rs1342193	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs1361684	0.80[EUR][1000 genomes]
rs1418296	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1418299	0.93[EUR][1000 genomes]
rs1418300	0.93[EUR][1000 genomes]
rs1418301	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1935416	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs1935417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1935418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4449673	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4540297	0.92[EUR][1000 genomes]
rs4706917	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6903637	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6913193	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82708200-82722400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:82709400-82723000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:82716000-82724400	Weak transcription	Right Atrium	heart

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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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