Variant report

Variant	rs62520863
Chromosome Location	chr8:124581848-124581849
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:124581720-124581870	GM12869	blood:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:124581523..124583761-chr8:124647181..124648699,2	MCF-7	breast:
2	chr8:124575939..124579271-chr8:124581722..124584580,4	MCF-7	breast:
3	chr8:124574833..124579835-chr8:124581420..124586695,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO32-2	chr8:124579311-124582785	ucscGeneNc_uc003yqp_1

No data

Variant related genes	Relation type
ENSG00000254113	TF binding region

Extended variants
information (count: 50 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs140613	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17254069	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17254421	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17255071	0.92[AMR][1000 genomes]
rs17255197	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs17337621	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs17338552	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17338860	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17339357	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17340040	0.92[AMR][1000 genomes]
rs62518433	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62518434	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62518437	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62518438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62518439	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62518440	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62518561	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62518563	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62518564	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62520862	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62520870	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62520871	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62520874	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62520906	0.90[EUR][1000 genomes]
rs62520908	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62520911	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62520913	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62520914	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62520917	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62520918	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62520919	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62520920	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62520921	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62520923	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62520926	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs62520927	1.00[AFR][1000 genomes]
rs62521279	1.00[AFR][1000 genomes]
rs62521284	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs62521286	0.81[EUR][1000 genomes]
rs62521287	0.81[EUR][1000 genomes]
rs62521289	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs62521291	1.00[AFR][1000 genomes]
rs62521292	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62523171	1.00[AFR][1000 genomes]
rs6999582	1.00[AFR][1000 genomes]
rs7004159	0.95[EUR][1000 genomes]
rs7827535	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs7827608	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7832861	1.00[AFR][1000 genomes];0.92[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	nsv831450	chr8:124471741-124661359	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124575600-124598600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:124578800-124582800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr8:124580600-124582000	Enhancers	Fetal Muscle Leg	muscle
4	chr8:124580600-124582400	Enhancers	Psoas Muscle	Psoas
5	chr8:124581400-124582600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr8:124581400-124583200	Weak transcription	Right Atrium	heart
7	chr8:124581400-124583200	Weak transcription	HSMMtube	muscle
8	chr8:124581400-124584600	Weak transcription	Placenta	Placenta
9	chr8:124581400-124584800	Weak transcription	Esophagus	oesophagus
10	chr8:124581400-124585000	Weak transcription	Adipose Nuclei	Adipose
11	chr8:124581600-124582600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr8:124581600-124586400	Weak transcription	Fetal Heart	heart

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