Variant report

Variant	rs7628279
Chromosome Location	chr3:56497855-56497856
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	chr3:56491622..56494953-chr3:56496657..56498979,3	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1388255	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1491163	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1552668	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1552669	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1878269	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35139577	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4527348	0.98[EUR][1000 genomes]
rs4974214	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58145335	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6445790	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6445792	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6762660	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6783666	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6784781	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6785094	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6796830	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6807444	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs725089	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7637479	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7644198	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7646515	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs975582	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9812701	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9829542	0.94[EUR][1000 genomes]
rs9856358	0.94[EUR][1000 genomes]
rs9871408	0.88[AMR][1000 genomes];0.98[EUR][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	esv3347557	chr3:56466500-56619322	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56493200-56500200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:56493200-56500800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr3:56493200-56501200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:56493600-56500600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr3:56494000-56500800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr3:56494200-56500800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:56494200-56500800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr3:56495000-56501000	Weak transcription	Gastric	stomach

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