Variant report

Variant	rs7146105
Chromosome Location	chr14:63219765-63219766
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10133621	0.90[ASN][1000 genomes]
rs12100978	0.81[ASN][1000 genomes]
rs12435061	0.80[EUR][1000 genomes]
rs1387754	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1490031	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1602211	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1826138	0.89[ASN][1000 genomes]
rs1844509	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1844510	0.82[EUR][1000 genomes]
rs2065632	0.87[EUR][1000 genomes]
rs4386055	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4441171	0.85[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63212800-63221600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:63218200-63220800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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