Variant report

Variant	rs73091003
Chromosome Location	chr1:212052731-212052732
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10449306	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28748135	1.00[ASN][1000 genomes]
rs28885134	1.00[ASN][1000 genomes]
rs4951551	1.00[ASN][1000 genomes]
rs56794231	1.00[ASN][1000 genomes]
rs56903779	1.00[ASN][1000 genomes]
rs57370359	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs57554409	1.00[ASN][1000 genomes]
rs59499736	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs60200148	1.00[ASN][1000 genomes]
rs61598472	1.00[ASN][1000 genomes]
rs6662642	1.00[ASN][1000 genomes]
rs6664087	1.00[ASN][1000 genomes]
rs7524573	1.00[ASN][1000 genomes]
rs7550801	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762218	chr1:212046447-212087682	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212052600-212052800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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