Variant report

Variant	rs428859
Chromosome Location	chr7:151019418-151019419
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12533535	1.00[ASN][1000 genomes]
rs12536027	1.00[ASN][1000 genomes]
rs13228980	1.00[ASN][1000 genomes]
rs13230325	1.00[ASN][1000 genomes]
rs13244540	1.00[ASN][1000 genomes]
rs35102612	1.00[ASN][1000 genomes]
rs35159986	1.00[ASN][1000 genomes]
rs35545989	1.00[ASN][1000 genomes]
rs35637117	1.00[ASN][1000 genomes]
rs432519	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs439031	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs445933	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73169681	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:151017200-151019600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:151017200-151025400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:151017400-151019800	ZNF genes & repeats	iPS DF 19.11 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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