Variant report

Variant	rs62491077
Chromosome Location	chr7:138113960-138113961
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:138113656..138118037-chr7:138143225..138147553,4	K562	blood:
2	chr7:138113307..138115089-chr7:138144254..138145776,2	K562	blood:

Variant related genes	Relation type
ENSG00000122779	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10225876	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10246196	0.87[EUR][1000 genomes]
rs10249638	0.81[ASN][1000 genomes]
rs10250362	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12533792	0.81[AMR][1000 genomes]
rs12668679	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12668708	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17169596	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17169597	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2353346	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2353348	0.83[ASN][1000 genomes]
rs2883142	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4574789	0.83[ASN][1000 genomes]
rs4620232	0.83[ASN][1000 genomes]
rs4626544	0.83[ASN][1000 genomes]
rs4732317	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55875241	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55924435	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56977478	0.81[AMR][1000 genomes]
rs62491063	0.85[AMR][1000 genomes]
rs62491064	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62491079	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62491082	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6467769	0.83[ASN][1000 genomes]
rs6467772	0.83[ASN][1000 genomes]
rs6947999	0.83[ASN][1000 genomes]
rs6953860	0.83[ASN][1000 genomes]
rs6962241	0.83[ASN][1000 genomes]
rs6962854	0.83[ASN][1000 genomes]
rs6964218	0.83[ASN][1000 genomes]
rs6968570	0.83[ASN][1000 genomes]
rs6973057	0.81[AMR][1000 genomes]
rs6980108	0.83[ASN][1000 genomes]
rs7793703	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831153	chr7:138078179-138265648	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138112600-138117000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr7:138113000-138115200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr7:138113800-138114800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:138113800-138117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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