Variant report

Variant	rs4732591
Chromosome Location	chr7:84498541-84498542
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:84491524..84493832-chr7:84496433..84498597,3	K562	blood:
2	chr7:84498248..84502734-chr7:84505735..84508151,4	K562	blood:
3	chr7:84474585..84476459-chr7:84497349..84500162,2	K562	blood:

Variant related genes	Relation type
ENSG00000232605	Chromatin interaction

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

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

rs_ID	r²[population]
rs10225298	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10225557	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10226229	1.00[TSI][hapmap]
rs10238680	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10244742	1.00[GIH][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap]
rs10253819	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10254761	0.97[ASN][1000 genomes]
rs10265448	0.81[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];0.97[ASN][1000 genomes]
rs10274814	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1318546	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13437628	0.97[ASN][1000 genomes]
rs1406341	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1583146	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1594395	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17159404	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159577	0.93[CHB][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes]
rs1811353	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1864526	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1864527	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1897156	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1997302	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2293574	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4128623	0.83[ASN][1000 genomes]
rs4283991	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4286890	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4549716	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4551285	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4563832	0.82[ASN][1000 genomes]
rs4595076	1.00[EUR][1000 genomes]
rs4728558	1.00[EUR][1000 genomes]
rs4728568	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.93[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4732580	0.84[AMR][1000 genomes]
rs4732583	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4732584	0.82[ASN][1000 genomes]
rs4732585	0.82[ASN][1000 genomes]
rs4732587	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4732590	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4732592	1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs57219677	0.84[AMR][1000 genomes]
rs58079066	0.87[ASN][1000 genomes]
rs58836788	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59138424	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59348972	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs61463020	1.00[EUR][1000 genomes]
rs6948339	0.81[ASN][1000 genomes]
rs73713541	0.98[ASN][1000 genomes]
rs73713553	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73713556	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs934302	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	esv34238	chr7:84279023-84591966	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv831050	chr7:84355996-84527261	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:84491400-84504400	Weak transcription	K562	blood

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