Variant report

Variant	rs9430000
Chromosome Location	chr1:209767699-209767700
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:209760979..209762618-chr1:209766680..209769028,3	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10489338	1.00[CHB][hapmap];0.88[JPT][hapmap];0.96[ASN][1000 genomes]
rs11119308	0.85[ASN][1000 genomes]
rs11119309	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.96[ASN][1000 genomes]
rs12058586	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12069172	1.00[CEU][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12074063	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12080730	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12094286	1.00[CEU][hapmap];0.81[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17014770	0.81[ASN][1000 genomes]
rs17014799	0.96[ASN][1000 genomes]
rs17014808	0.96[ASN][1000 genomes]
rs17014825	0.88[CHB][hapmap];0.81[ASN][1000 genomes]
rs17014842	1.00[ASW][hapmap];1.00[CEU][hapmap];0.84[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.81[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2067744	0.81[ASN][1000 genomes]
rs2072908	1.00[CEU][hapmap];0.85[CHB][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2076225	1.00[CEU][hapmap];0.89[CHB][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2235451	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60686175	0.81[ASN][1000 genomes]
rs6659229	0.81[AFR][1000 genomes]
rs6663545	0.81[ASN][1000 genomes]
rs6690557	0.95[CHB][hapmap]
rs7512091	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs7553109	0.81[AFR][1000 genomes]
rs926385	0.81[ASN][1000 genomes]
rs9429821	0.95[CHB][hapmap]
rs9429822	1.00[CEU][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9430001	1.00[CHB][hapmap]
rs9430005	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999901	chr1:209600631-210205379	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1014034	chr1:209759648-210501731	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9430000	CCDC18	Cis_chr	lymphoblastoid	RTeQTL

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209760600-209776400	Weak transcription	Fetal Lung	lung
2	chr1:209764200-209776600	Weak transcription	Ovary	ovary
3	chr1:209764200-209780400	Weak transcription	Fetal Brain Male	brain
4	chr1:209764600-209791200	Weak transcription	Brain Anterior Caudate	brain
5	chr1:209765000-209768400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:209765400-209776800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr1:209766000-209768800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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