Variant report

Variant	rs72968770
Chromosome Location	chr11:93843066-93843067
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:93839493..93841789-chr11:93842574..93845095,2	K562	blood:
2	chr11:93843038..93846219-chr11:93861023..93863615,3	MCF-7	breast:
3	chr11:93834842..93837359-chr11:93842691..93845268,2	K562	blood:

Variant related genes	Relation type
ENSG00000110218	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11828881	0.87[ASN][1000 genomes]
rs56723829	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58049964	0.85[ASN][1000 genomes]
rs58216749	0.94[ASN][1000 genomes]
rs58863592	0.85[ASN][1000 genomes]
rs58965645	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59768849	0.85[ASN][1000 genomes]
rs67060752	0.85[ASN][1000 genomes]
rs7102046	0.85[ASN][1000 genomes]
rs7120920	0.85[ASN][1000 genomes]
rs72968735	0.88[ASN][1000 genomes]
rs72968739	0.97[ASN][1000 genomes]
rs72968751	0.97[ASN][1000 genomes]
rs72968772	0.97[ASN][1000 genomes]
rs72968780	0.97[ASN][1000 genomes]
rs72968785	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72968788	0.91[ASN][1000 genomes]
rs72968791	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs72970708	0.87[ASN][1000 genomes]
rs72970709	0.87[ASN][1000 genomes]
rs72970719	0.85[ASN][1000 genomes]
rs72970727	0.85[ASN][1000 genomes]
rs73512252	0.85[ASN][1000 genomes]
rs7925027	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898183	chr11:93725384-93906735	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv898184	chr11:93741612-93969726	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1046092	chr11:93833446-93964452	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv523082	chr11:93834223-93866147	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv508651	chr11:93834300-93880470	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr11:93838600-93845000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:93838600-93845000	Weak transcription	NHEK	skin
3	chr11:93838800-93844800	Weak transcription	HMEC	breast
4	chr11:93840200-93843200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:93840200-93845000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:93840400-93844600	Weak transcription	HSMMtube	muscle
7	chr11:93843000-93845000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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