Variant report

Variant	rs11854306
Chromosome Location	chr15:40023237-40023238
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:40022385..40024167-chr15:40025741..40027363,2	K562	blood:
2	chr15:40021204..40023885-chr15:40025697..40027241,2	K562	blood:
3	chr15:40021277..40023471-chr15:40056551..40058310,2	MCF-7	breast:
4	chr15:40013365..40015797-chr15:40023109..40026262,4	K562	blood:
5	chr15:40013612..40015797-chr15:40023109..40024844,3	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11855578	0.99[ASN][1000 genomes]
rs1320036	0.94[ASN][1000 genomes]
rs1906153	0.91[ASN][1000 genomes]
rs1906159	0.99[ASN][1000 genomes]
rs1906160	0.92[ASN][1000 genomes]
rs2087133	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2129458	0.88[ASN][1000 genomes]
rs2171310	0.98[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2254829	0.91[ASN][1000 genomes]
rs2254942	0.91[ASN][1000 genomes]
rs2254947	0.91[ASN][1000 genomes]
rs2412424	0.88[ASN][1000 genomes]
rs2631692	0.90[ASN][1000 genomes]
rs2631693	0.90[ASN][1000 genomes]
rs2631694	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2631695	0.91[ASN][1000 genomes]
rs2631696	0.91[ASN][1000 genomes]
rs2631698	0.91[ASN][1000 genomes]
rs2631703	0.94[ASN][1000 genomes]
rs2631708	0.88[ASN][1000 genomes]
rs2631709	0.88[ASN][1000 genomes]
rs2631711	0.89[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2631712	0.89[ASN][1000 genomes]
rs2631713	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2631715	0.89[ASN][1000 genomes]
rs2664124	0.88[ASN][1000 genomes]
rs2664126	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2664127	0.89[ASN][1000 genomes]
rs2664129	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2664130	0.91[ASN][1000 genomes]
rs2664131	0.91[ASN][1000 genomes]
rs2664132	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3103066	0.90[ASN][1000 genomes]
rs62004771	0.95[ASN][1000 genomes]
rs62004772	0.99[ASN][1000 genomes]
rs67426899	0.95[ASN][1000 genomes]
rs7171939	0.96[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs8028503	0.89[ASN][1000 genomes]
rs8035895	0.89[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	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv832978	chr15:39899759-40094881	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40021800-40038000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:40022800-40023400	Enhancers	Rectal Mucosa Donor 29	rectum
3	chr15:40023200-40024200	Enhancers	A549	lung
4	chr15:40023200-40024800	Weak transcription	HepG2	liver
5	chr15:40023200-40027000	Weak transcription	Rectal Mucosa Donor 31	rectum

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