Variant report

Variant	rs7786846
Chromosome Location	chr7:66853707-66853708
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	chr7:66827114..66829996-chr7:66851331..66853827,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11760794	0.95[ASN][1000 genomes]
rs11760843	1.00[CHB][hapmap];0.84[JPT][hapmap];0.90[ASN][1000 genomes]
rs11760899	0.95[ASN][1000 genomes]
rs11762397	0.95[ASN][1000 genomes]
rs11763894	0.90[ASN][1000 genomes]
rs11768598	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769438	0.86[ASN][1000 genomes]
rs11770307	0.93[ASN][1000 genomes]
rs11771920	0.89[ASN][1000 genomes]
rs11772041	1.00[CHB][hapmap];0.92[ASN][1000 genomes]
rs11772331	0.92[ASN][1000 genomes]
rs11773173	0.92[ASN][1000 genomes]
rs12698575	0.92[ASN][1000 genomes]
rs13226941	1.00[CHB][hapmap];0.92[ASN][1000 genomes]
rs13241524	0.92[ASN][1000 genomes]
rs13241865	0.92[ASN][1000 genomes]
rs17137359	0.92[ASN][1000 genomes]
rs17144911	0.92[CEU][hapmap]
rs1968150	0.95[ASN][1000 genomes]
rs34037266	0.95[ASN][1000 genomes]
rs34671876	0.92[ASN][1000 genomes]
rs35307336	0.87[ASN][1000 genomes]
rs35565843	0.98[ASN][1000 genomes]
rs35715970	0.95[ASN][1000 genomes]
rs36146582	1.00[ASN][1000 genomes]
rs4236211	0.98[ASN][1000 genomes]
rs4590320	0.97[ASN][1000 genomes]
rs4717364	0.92[ASN][1000 genomes]
rs4718534	0.92[ASN][1000 genomes]
rs4718536	0.92[ASN][1000 genomes]
rs4718559	0.95[ASN][1000 genomes]
rs4718560	0.89[ASN][1000 genomes]
rs55777645	0.92[ASN][1000 genomes]
rs62466443	0.92[ASN][1000 genomes]
rs62467577	0.98[ASN][1000 genomes]
rs6956666	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6960865	0.92[ASN][1000 genomes]
rs6963583	0.92[ASN][1000 genomes]
rs71565103	0.90[ASN][1000 genomes]
rs71565104	0.90[ASN][1000 genomes]
rs7341400	0.89[ASN][1000 genomes]
rs7788177	0.92[ASN][1000 genomes]
rs7804093	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs887715	0.90[ASN][1000 genomes]
rs9443	0.92[ASN][1000 genomes]
rs956523	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758118	chr7:66401430-66859253	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	esv2759535	chr7:66401430-66859253	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv888330	chr7:66502171-66877880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
4	nsv1031147	chr7:66811313-66922350	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1025049	chr7:66823977-66906930	Bivalent Enhancer Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:15)

SNP	Gene	Cis/trans	Tissue	Source
rs7786846	STAG3L4	cis	Muscle Skeletal	GTEx
rs7786846	STAG3L4	cis	Adipose Subcutaneous	GTEx
rs7786846	FLJ13195	Cis_1M	lymphoblastoid	RTeQTL
rs7786846	STAG3L4	cis	Thyroid	GTEx
rs7786846	STAG3L4	cis	Esophagus Mucosa	GTEx
rs7786846	STAG3L4	cis	lung	GTEx
rs7786846	STAG3L4	cis	Nerve Tibial	GTEx
rs7786846	STAG3L4	cis	Artery Tibial	GTEx
rs7786846	STAG3L4	cis	Whole Blood	GTEx
rs7786846	STAG3L4	cis	Esophagus Muscularis	GTEx
rs7786846	FLJ13195	cis	normal skin	skin_eQTL
rs7786846	FLJ13195	cis	lesional skin	skin_eQTL
rs7786846	STAG3L4	cis	Artery Aorta	GTEx
rs7786846	FLJ13195	cis	uninvolved skin	skin_eQTL
rs7786846	STAG3L4	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66853600-66853800	Enhancers	H1 Cell Line	embryonic stem cell
2	chr7:66853600-66853800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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