Variant report

Variant	rs72907786
Chromosome Location	chr11:19130770-19130771
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:19096399..19098941-chr11:19128925..19131186,2	MCF-7	breast:
2	chr11:19130172..19132121-chr11:19136917..19138770,2	MCF-7	breast:
3	chr11:19126978..19129301-chr11:19130674..19132718,2	K562	blood:
4	chr11:19130396..19132197-chr11:19136477..19139214,2	K562	blood:

Variant related genes	Relation type
ENSG00000177054	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10444252	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10444253	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10444255	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10500837	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024985	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11024986	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11024987	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11024988	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11024989	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024990	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024991	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024992	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024993	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024994	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024995	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024996	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024998	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11024999	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11025002	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11025004	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11025005	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11025006	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11025007	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11025008	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16936140	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59840223	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72889769	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72889773	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72889781	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72889786	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72889799	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72889802	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72891506	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72891507	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72891510	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72907780	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72907782	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72907784	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9299952	0.96[AMR][1000 genomes];0.97[EUR][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	nsv1040805	chr11:19037871-19892803	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv540957	chr11:19037871-19892803	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:19125000-19138600	Weak transcription	Gastric	stomach
2	chr11:19129400-19133400	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr11:19130200-19131000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:19130400-19131000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:19130400-19131400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:19130600-19131200	Enhancers	Esophagus	oesophagus
7	chr11:19130600-19131400	Enhancers	Monocytes-CD14+_RO01746	blood

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