Variant report

Variant	rs35909486
Chromosome Location	chr15:45576115-45576116
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:45569531..45573804-chr15:45574479..45576366,3	K562	blood:
2	chr15:45569684..45572430-chr15:45574866..45576631,2	K562	blood:

Variant related genes	Relation type
ENSG00000259520	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10519018	0.89[ASN][1000 genomes]
rs1060896	0.89[ASN][1000 genomes]
rs11629807	0.89[ASN][1000 genomes]
rs11629858	0.89[ASN][1000 genomes]
rs11629859	0.89[ASN][1000 genomes]
rs11631021	0.89[ASN][1000 genomes]
rs11632419	0.89[ASN][1000 genomes]
rs11632651	0.89[ASN][1000 genomes]
rs11632724	0.89[ASN][1000 genomes]
rs11632752	0.89[ASN][1000 genomes]
rs11632778	0.89[ASN][1000 genomes]
rs11632920	0.89[ASN][1000 genomes]
rs11637364	0.89[ASN][1000 genomes]
rs11637838	0.89[ASN][1000 genomes]
rs11637920	0.89[ASN][1000 genomes]
rs11639349	0.89[ASN][1000 genomes]
rs11639420	0.89[ASN][1000 genomes]
rs11639483	0.86[ASN][1000 genomes]
rs11854325	0.89[ASN][1000 genomes]
rs11854365	0.89[ASN][1000 genomes]
rs12440356	0.89[ASN][1000 genomes]
rs12898652	0.82[ASN][1000 genomes]
rs12898818	0.89[ASN][1000 genomes]
rs12899058	0.89[ASN][1000 genomes]
rs12899942	0.89[ASN][1000 genomes]
rs12904150	0.89[ASN][1000 genomes]
rs12908818	0.89[ASN][1000 genomes]
rs12910009	0.89[ASN][1000 genomes]
rs12911111	0.89[ASN][1000 genomes]
rs12911186	0.89[ASN][1000 genomes]
rs12913500	0.83[ASN][1000 genomes]
rs12915314	0.89[ASN][1000 genomes]
rs1706767	0.86[ASN][1000 genomes]
rs1706768	0.89[ASN][1000 genomes]
rs1706770	0.89[ASN][1000 genomes]
rs1719232	0.89[ASN][1000 genomes]
rs1719236	0.89[ASN][1000 genomes]
rs2271438	0.89[ASN][1000 genomes]
rs2413768	0.86[ASN][1000 genomes]
rs2413771	0.89[ASN][1000 genomes]
rs2413772	0.89[ASN][1000 genomes]
rs2413773	0.89[ASN][1000 genomes]
rs2413774	0.89[ASN][1000 genomes]
rs2458225	0.89[ASN][1000 genomes]
rs2461705	0.89[ASN][1000 genomes]
rs2687511	0.89[ASN][1000 genomes]
rs4533219	0.89[ASN][1000 genomes]
rs6493143	0.89[ASN][1000 genomes]
rs6493144	0.89[ASN][1000 genomes]
rs6493145	0.89[ASN][1000 genomes]
rs7162022	0.89[ASN][1000 genomes]
rs7165039	0.89[ASN][1000 genomes]
rs7166580	0.89[ASN][1000 genomes]
rs7167146	0.89[ASN][1000 genomes]
rs7171312	0.89[ASN][1000 genomes]
rs8024620	0.89[ASN][1000 genomes]
rs8037583	0.81[ASN][1000 genomes]
rs8039138	0.89[ASN][1000 genomes]
rs8039153	0.86[ASN][1000 genomes]
rs8039352	0.89[ASN][1000 genomes]
rs8039354	0.89[ASN][1000 genomes]
rs8039540	0.89[ASN][1000 genomes]
rs8040185	0.89[ASN][1000 genomes]
rs8041702	0.89[ASN][1000 genomes]
rs8041874	0.89[ASN][1000 genomes]
rs9920290	0.89[ASN][1000 genomes]
rs9921025	0.89[ASN][1000 genomes]
rs9921035	0.89[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	nsv916374	chr15:45058112-45769052	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv932147	chr15:45319178-45872076	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv869616	chr15:45401411-45736209	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats 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
4	nsv569315	chr15:45446156-45772448	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs35909486	CTD-2651B20.3	cis	lung	GTEx
rs35909486	CTD-2651B20.3	cis	Artery Tibial	GTEx
rs35909486	CTD-2651B20.3	cis	Heart Left Ventricle	GTEx
rs35909486	CTD-2651B20.4	cis	Nerve Tibial	GTEx
rs35909486	CTD-2651B20.3	cis	Artery Aorta	GTEx
rs35909486	CTD-2651B20.4	cis	Artery Tibial	GTEx
rs35909486	CTD-2651B20.3	cis	Adipose Subcutaneous	GTEx
rs35909486	CTD-2651B20.3	cis	Nerve Tibial	GTEx
rs35909486	CTD-2651B20.3	cis	Thyroid	GTEx
rs35909486	CTD-2651B20.4	cis	Skin Sun Exposed Lower leg	GTEx
rs35909486	CTD-2651B20.3	cis	Esophagus Muscularis	GTEx
rs35909486	CTD-2651B20.3	cis	Muscle Skeletal	GTEx
rs35909486	CTD-2651B20.3	cis	Skin Sun Exposed Lower leg	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45572200-45592000	Weak transcription	Right Atrium	heart
2	chr15:45572400-45577600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr15:45572600-45577800	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr15:45572800-45576400	Weak transcription	Fetal Intestine Large	intestine
5	chr15:45572800-45576400	Weak transcription	Fetal Intestine Small	intestine
6	chr15:45572800-45584200	Weak transcription	Psoas Muscle	Psoas
7	chr15:45575800-45576600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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