Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10133987	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10134175	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10137794	0.96[ASN][1000 genomes]
rs10141070	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs11159286	0.83[AMR][1000 genomes]
rs12882571	0.91[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs176942	0.87[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs176949	0.91[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs176967	1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28481884	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28640141	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs28648386	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4622441	0.87[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4903625	0.83[AMR][1000 genomes]
rs61990714	1.00[ASN][1000 genomes]
rs6574389	0.80[ASN][1000 genomes]
rs6574403	0.96[ASN][1000 genomes]
rs7144053	0.95[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7148286	0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7151514	0.95[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs8021036	0.91[AMR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758362	chr14:78074180-78262572	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	esv2759998	chr14:78074180-78262572	Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1043788	chr14:78178490-78381190	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	esv2754594	chr14:78222798-78275549	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78252800-78255400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:78252800-78256800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr14:78253200-78256800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr14:78253600-78260800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:78253600-78261800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr14:78253800-78256600	Weak transcription	Hela-S3	cervix
7	chr14:78253800-78266200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:78254000-78256600	Weak transcription	Placenta	Placenta

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