Variant report

Variant	rs73281578
Chromosome Location	chr7:26268273-26268274
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:26264944..26269411-chr7:26271186..26275116,6	K562	blood:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10499571	0.85[ASN][1000 genomes]
rs11971108	0.94[EUR][1000 genomes]
rs11971308	0.89[EUR][1000 genomes]
rs11971320	0.89[EUR][1000 genomes]
rs11972057	0.89[EUR][1000 genomes]
rs11975011	0.89[EUR][1000 genomes]
rs11976883	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11977822	0.89[EUR][1000 genomes]
rs12669191	0.92[ASN][1000 genomes]
rs12669830	0.85[ASN][1000 genomes]
rs16870111	0.85[ASN][1000 genomes]
rs17153368	0.85[ASN][1000 genomes]
rs17153396	0.85[ASN][1000 genomes]
rs41275982	0.89[EUR][1000 genomes]
rs55754901	0.89[EUR][1000 genomes]
rs55813103	0.86[EUR][1000 genomes]
rs56021640	0.89[EUR][1000 genomes]
rs56132015	0.86[EUR][1000 genomes]
rs56276467	0.89[EUR][1000 genomes]
rs56287413	0.84[EUR][1000 genomes]
rs56376224	0.84[EUR][1000 genomes]
rs56393994	0.89[EUR][1000 genomes]
rs56413126	0.84[EUR][1000 genomes]
rs59142558	0.89[EUR][1000 genomes]
rs59685141	0.89[EUR][1000 genomes]
rs60954252	1.00[EUR][1000 genomes]
rs61009175	0.89[EUR][1000 genomes]
rs73281517	0.86[EUR][1000 genomes]
rs73281521	0.89[EUR][1000 genomes]
rs73281523	0.89[EUR][1000 genomes]
rs73281527	0.89[EUR][1000 genomes]
rs73281529	0.89[EUR][1000 genomes]
rs73281530	0.89[EUR][1000 genomes]
rs73281532	0.89[EUR][1000 genomes]
rs73281538	0.89[EUR][1000 genomes]
rs73281546	0.89[EUR][1000 genomes]
rs73281548	0.89[EUR][1000 genomes]
rs73281550	0.89[EUR][1000 genomes]
rs73281551	0.89[EUR][1000 genomes]
rs73281554	0.89[EUR][1000 genomes]
rs73281562	0.89[EUR][1000 genomes]
rs73281563	0.89[EUR][1000 genomes]
rs73281570	0.89[EUR][1000 genomes]
rs73281586	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73281591	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7793815	0.89[EUR][1000 genomes]
rs7793849	0.89[EUR][1000 genomes]
rs7794892	0.98[ASN][1000 genomes]
rs7798249	1.00[EUR][1000 genomes]
rs7807030	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021308	chr7:26116605-26419720	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv1018971	chr7:26161228-26380361	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	esv1821097	chr7:26243108-26303403	Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr7:26244400-26271400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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