Variant report

Variant	rs582773
Chromosome Location	chr1:73938694-73938695
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:73938555..73940544-chr1:73941674..73943593,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10518424	0.95[EUR][1000 genomes]
rs11210253	1.00[EUR][1000 genomes]
rs11804961	1.00[EUR][1000 genomes]
rs12121257	0.95[EUR][1000 genomes]
rs12122713	0.95[EUR][1000 genomes]
rs12122747	0.94[EUR][1000 genomes]
rs12124740	0.95[EUR][1000 genomes]
rs12126028	0.95[EUR][1000 genomes]
rs12126048	0.95[EUR][1000 genomes]
rs12126645	0.95[EUR][1000 genomes]
rs12127373	0.95[EUR][1000 genomes]
rs12128002	0.93[EUR][1000 genomes]
rs12129139	0.95[EUR][1000 genomes]
rs12129351	0.95[EUR][1000 genomes]
rs12129496	0.95[EUR][1000 genomes]
rs12130189	0.95[EUR][1000 genomes]
rs12131271	0.95[EUR][1000 genomes]
rs12133609	0.94[EUR][1000 genomes]
rs12134765	0.95[EUR][1000 genomes]
rs12134933	0.95[EUR][1000 genomes]
rs12139822	0.93[EUR][1000 genomes]
rs12139989	0.93[EUR][1000 genomes]
rs12140132	0.95[EUR][1000 genomes]
rs12145235	1.00[EUR][1000 genomes]
rs17512311	0.95[EUR][1000 genomes]
rs17568889	0.89[EUR][1000 genomes]
rs17571591	0.95[EUR][1000 genomes]
rs17571689	0.95[EUR][1000 genomes]
rs17571745	0.95[EUR][1000 genomes]
rs28565938	0.95[EUR][1000 genomes]
rs55811030	0.95[EUR][1000 genomes]
rs59126753	0.95[EUR][1000 genomes]
rs59403678	0.89[EUR][1000 genomes]
rs6687434	0.87[EUR][1000 genomes]
rs74091630	1.00[EUR][1000 genomes]
rs74091667	0.95[EUR][1000 genomes]
rs74091844	1.00[EUR][1000 genomes]
rs74093919	0.91[EUR][1000 genomes]
rs74093920	0.93[EUR][1000 genomes]
rs74093921	0.95[EUR][1000 genomes]
rs74093923	0.95[EUR][1000 genomes]
rs74094852	0.89[EUR][1000 genomes]
rs7526312	0.95[EUR][1000 genomes]
rs7526580	0.95[EUR][1000 genomes]
rs7528347	0.87[EUR][1000 genomes]
rs7535708	0.95[EUR][1000 genomes]
rs7537989	0.95[EUR][1000 genomes]
rs7545661	0.95[EUR][1000 genomes]
rs7546663	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005356	chr1:73542786-74124065	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv870536	chr1:73647909-74031554	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73938600-73943200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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