Variant report

Variant	rs7579946
Chromosome Location	chr2:86043673-86043674
allele	A/G
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]
rs1105882	0.88[CEU][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11690161	0.92[CEU][hapmap];0.91[JPT][hapmap];0.88[EUR][1000 genomes]
rs13420465	0.84[ASN][1000 genomes]
rs1518987	0.85[CEU][hapmap]
rs1607466	0.83[ASN][1000 genomes]
rs2049015	0.84[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.88[ASN][1000 genomes]
rs2366946	0.83[ASN][1000 genomes]
rs7564431	0.89[ASN][1000 genomes]
rs7576320	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86029800-86054400	Weak transcription	Spleen	Spleen
2	chr2:86039800-86074800	Weak transcription	Aorta	Aorta
3	chr2:86041400-86045200	Weak transcription	Ovary	ovary
4	chr2:86041400-86049600	Weak transcription	Lung	lung
5	chr2:86042200-86054800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:86042600-86047400	Weak transcription	A549	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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