Variant report

Variant	rs62086078
Chromosome Location	chr18:9451683-9451684
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	chr18:9442961..9446993-chr18:9449130..9451734,3	K562	blood:
2	chr18:9450353..9452789-chr18:9457318..9459347,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs16955192	0.81[AMR][1000 genomes]
rs3322	0.81[AMR][1000 genomes]
rs62086074	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62086075	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62086079	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086080	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62086098	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086099	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086100	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086104	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086106	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086107	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086109	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62086112	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62086113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62086116	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62086122	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62086123	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62086125	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62086148	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62086149	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62086157	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62087360	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62087361	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62087362	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62087369	0.81[AMR][1000 genomes]
rs62087374	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62087376	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs62087397	0.81[AMR][1000 genomes]
rs7227801	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7233885	0.97[EUR][1000 genomes]
rs7235785	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916373	chr18:9026803-9592201	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv1056407	chr18:9144345-9553764	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv1062025	chr18:9287249-9552470	Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv543643	chr18:9287249-9552470	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv833585	chr18:9401630-9597291	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv428005	chr18:9401658-9542396	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs62086078	RALBP1	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9446800-9453800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr18:9450200-9453600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr18:9450400-9453400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr18:9450400-9453600	Weak transcription	Fetal Brain Female	brain
5	chr18:9450400-9453800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr18:9450600-9453800	Weak transcription	K562	blood
7	chr18:9450800-9453800	Weak transcription	Fetal Brain Male	brain
8	chr18:9451000-9453800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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