Variant report

Variant	rs7769542
Chromosome Location	chr6:150717788-150717789
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:150717285..150719589-chr6:150720584..150722449,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11962096	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12530375	0.98[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1339110	0.84[AMR][1000 genomes]
rs1416481	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1556881	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2076285	0.96[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2076286	0.96[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2076287	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2076288	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2076289	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2076290	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2076291	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2076292	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3734734	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3823259	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3823260	0.94[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4407723	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4479949	0.81[ASN][1000 genomes]
rs62432506	0.87[AMR][1000 genomes]
rs62432511	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs62432540	0.96[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs62432541	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs62432542	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6909655	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6921360	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73617698	0.94[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7745569	0.91[AMR][1000 genomes]
rs7761906	0.91[AMR][1000 genomes]
rs7762616	0.93[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7770389	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7774077	0.96[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7774404	0.87[ASN][1000 genomes]
rs9322259	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9371437	0.84[ASN][1000 genomes]
rs9384472	0.91[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs9384473	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9384474	0.82[ASN][1000 genomes]
rs9384476	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9397302	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9397303	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9397944	0.84[ASN][1000 genomes]
rs9397954	0.81[AMR][1000 genomes];0.95[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	esv2763602	chr6:150581193-150720666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150712200-150719200	Weak transcription	Fetal Intestine Small	intestine
2	chr6:150716400-150718200	Weak transcription	Liver	Liver

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