Variant report

Variant	rs12442435
Chromosome Location	chr15:78044631-78044632
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:78044160..78046640-chr15:78075370..78077627,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10851897	0.80[ASN][1000 genomes]
rs10851898	0.90[ASN][1000 genomes]
rs11072670	0.90[ASN][1000 genomes]
rs11629474	0.90[ASN][1000 genomes]
rs11631237	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11632255	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11635700	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11636173	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11636649	0.81[ASN][1000 genomes]
rs11637968	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12438542	0.80[ASN][1000 genomes]
rs28702419	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3935682	0.82[ASN][1000 genomes]
rs3935683	0.82[ASN][1000 genomes]
rs3935684	0.81[ASN][1000 genomes]
rs3935685	0.82[ASN][1000 genomes]
rs3935831	0.80[ASN][1000 genomes]
rs4072803	0.85[ASN][1000 genomes]
rs4886904	0.80[ASN][1000 genomes]
rs58619842	0.90[ASN][1000 genomes]
rs58813188	0.82[ASN][1000 genomes]
rs58831466	0.80[ASN][1000 genomes]
rs60917280	0.82[ASN][1000 genomes]
rs62007780	0.80[ASN][1000 genomes]
rs62007781	0.80[ASN][1000 genomes]
rs62007784	0.82[ASN][1000 genomes]
rs72730707	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72730712	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72730714	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	nsv833061	chr15:77998374-78121905	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv904420	chr15:78025267-78078903	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv833062	chr15:78035206-78220358	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv904421	chr15:78041789-78129964	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr15:78036800-78045800	Weak transcription	Right Atrium	heart
2	chr15:78040400-78045200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr15:78040400-78046200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr15:78043400-78045000	Weak transcription	Spleen	Spleen
5	chr15:78044400-78046200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:78044400-78047400	Enhancers	Fetal Brain Female	brain
7	chr15:78044600-78044800	Bivalent Enhancer	Brain Germinal Matrix	brain

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