Variant report

Variant	rs11768598
Chromosome Location	chr7:66844253-66844254
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs11531446	0.81[EUR][1000 genomes]
rs11543607	0.80[EUR][1000 genomes]
rs11760794	0.95[ASN][1000 genomes]
rs11760843	0.90[ASN][1000 genomes]
rs11760899	0.95[ASN][1000 genomes]
rs11762397	0.95[ASN][1000 genomes]
rs11763894	0.90[ASN][1000 genomes]
rs11768377	0.80[EUR][1000 genomes]
rs11769438	0.86[ASN][1000 genomes]
rs11770307	0.93[ASN][1000 genomes]
rs11771920	0.89[ASN][1000 genomes]
rs11772041	0.92[ASN][1000 genomes]
rs11772331	0.92[ASN][1000 genomes]
rs11773173	0.92[ASN][1000 genomes]
rs12698575	0.92[ASN][1000 genomes]
rs13226941	0.92[ASN][1000 genomes]
rs13230948	0.80[EUR][1000 genomes]
rs13238678	0.81[EUR][1000 genomes]
rs13241524	0.92[ASN][1000 genomes]
rs13241865	0.92[ASN][1000 genomes]
rs17137359	0.92[ASN][1000 genomes]
rs17144911	0.80[EUR][1000 genomes]
rs1968150	0.95[ASN][1000 genomes]
rs2421294	0.80[EUR][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	0.92[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]
rs7786846	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7788177	0.92[ASN][1000 genomes]
rs7804093	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[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];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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	nsv1031560	chr7:66805244-66846663	Enhancers Strong transcription Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1022779	chr7:66805244-66849392	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	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
7	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
8	esv3374929	chr7:66843317-66848115	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv33458	chr7:66843998-66849444	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3430927	chr7:66844117-66847215	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3342206	chr7:66844217-66847215	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs11768598	STAG3L4	cis	Muscle Skeletal	GTEx
rs11768598	STAG3L4	cis	Thyroid	GTEx
rs11768598	STAG3L4	cis	Whole Blood	GTEx
rs11768598	STAG3L4	cis	Artery Aorta	GTEx
rs11768598	STAG3L4	cis	Esophagus Mucosa	GTEx
rs11768598	STAG3L4	cis	Nerve Tibial	GTEx
rs11768598	STAG3L4	cis	Adipose Subcutaneous	GTEx
rs11768598	STAG3L4	cis	Esophagus Muscularis	GTEx
rs11768598	STAG3L4	cis	lung	GTEx
rs11768598	FLJ13195	Cis_1M	lymphoblastoid	RTeQTL
rs11768598	STAG3L4	cis	Artery Tibial	GTEx
rs11768598	STAG3L4	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66843000-66847200	Enhancers	Fetal Stomach	stomach
2	chr7:66843800-66844800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr7:66843800-66845000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr7:66843800-66845000	Weak transcription	Fetal Lung	lung
5	chr7:66843800-66845400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:66843800-66845400	Weak transcription	Spleen	Spleen
7	chr7:66844000-66845000	Weak transcription	Colon Smooth Muscle	Colon
8	chr7:66844000-66845000	Weak transcription	Ovary	ovary
9	chr7:66844200-66844800	Weak transcription	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links