Variant report

Variant	rs11204743
Chromosome Location	chr1:150890406-150890407
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:150888318..150890863-chr1:150893491..150895097,2	K562	blood:
2	chr1:150889960..150892328-chr1:150896397..150898404,2	MCF-7	breast:
3	chr1:150888096..150891022-chr1:150892225..150894393,2	K562	blood:

Extended variants
information (count: 94 )
Associated
traits (count: 25 )

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1027699	0.81[EUR][1000 genomes]
rs10305664	0.82[EUR][1000 genomes]
rs10305673	0.81[EUR][1000 genomes]
rs10305704	0.81[EUR][1000 genomes]
rs10305711	0.81[EUR][1000 genomes]
rs10305714	0.81[EUR][1000 genomes]
rs10399947	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10888397	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10888398	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11204733	0.80[EUR][1000 genomes]
rs11204739	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11204742	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11204747	0.98[ASN][1000 genomes]
rs11204748	0.98[ASN][1000 genomes]
rs11204749	0.96[ASN][1000 genomes]
rs11204750	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11552229	0.81[EUR][1000 genomes]
rs11579736	0.82[ASN][1000 genomes]
rs11581757	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11582281	0.80[EUR][1000 genomes]
rs11583707	0.84[ASN][1000 genomes]
rs11589458	0.81[EUR][1000 genomes]
rs11589886	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12059949	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12067685	0.84[ASN][1000 genomes]
rs12075597	0.90[ASN][1000 genomes]
rs12090215	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12096831	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12097963	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12405726	0.83[ASN][1000 genomes]
rs12409208	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12410394	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12410869	0.81[ASN][1000 genomes]
rs12562939	0.84[ASN][1000 genomes]
rs1546376	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17660092	0.81[EUR][1000 genomes]
rs1889741	0.92[ASN][1000 genomes]
rs1972060	0.95[ASN][1000 genomes]
rs2004903	0.92[ASN][1000 genomes]
rs2089082	0.81[EUR][1000 genomes]
rs2124952	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2271076	0.98[ASN][1000 genomes]
rs2272214	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2280627	0.95[ASN][1000 genomes]
rs2864882	0.94[ASN][1000 genomes]
rs2867296	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2867297	0.89[ASN][1000 genomes]
rs34985895	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35309985	0.83[ASN][1000 genomes]
rs36008098	0.81[ASN][1000 genomes]
rs3768015	0.81[EUR][1000 genomes]
rs3768016	0.81[EUR][1000 genomes]
rs3843843	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3849279	0.87[ASN][1000 genomes]
rs4451553	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4970928	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4970929	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4970930	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4970931	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4970980	0.90[ASN][1000 genomes]
rs4970982	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4970984	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4970985	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4970986	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4970987	0.85[ASN][1000 genomes]
rs4970988	0.84[ASN][1000 genomes]
rs59024312	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6587542	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6658066	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6660845	0.84[EUR][1000 genomes]
rs6669855	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6677420	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs66847267	0.94[ASN][1000 genomes]
rs6686064	0.88[ASN][1000 genomes]
rs72704652	0.81[EUR][1000 genomes]
rs72704654	0.81[EUR][1000 genomes]
rs72704658	0.81[EUR][1000 genomes]
rs72704679	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs72704682	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72704685	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7518156	0.88[ASN][1000 genomes]
rs7521592	0.81[EUR][1000 genomes]
rs752376	0.95[ASN][1000 genomes]
rs7528773	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7556451	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7556661	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8444	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs897815	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9661876	0.82[AMR][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	esv2829859	chr1:150608894-150937329	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1001897	chr1:150743271-151241600	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
3	nsv535158	chr1:150743271-151241600	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
4	nsv1008496	chr1:150845827-150970656	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
5	nsv947130	chr1:150878115-150899504	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:25)

SNP	Gene	Cis/trans	Tissue	Source
rs11204743	HORMAD1	cis	Nerve Tibial	GTEx
rs11204743	RP11-316M1.12	cis	Muscle Skeletal	GTEx
rs11204743	CTSS	cis	Thyroid	GTEx
rs11204743	HORMAD1	cis	Esophagus Mucosa	GTEx
rs11204743	RP11-316M1.12	cis	Thyroid	GTEx
rs11204743	HORMAD1	cis	Skin Sun Exposed Lower leg	GTEx
rs11204743	CTSS	cis	multi-tissue	Pritchard
rs11204743	RP11-316M1.12	cis	Whole Blood	GTEx
rs11204743	RP11-316M1.12	cis	lung	GTEx
rs11204743	ARNT	Cis_1M	lymphoblastoid	RTeQTL
rs11204743	RP11-316M1.12	cis	Adipose Subcutaneous	GTEx
rs11204743	RP11-316M1.12	cis	Heart Left Ventricle	GTEx
rs11204743	RNU6-1042P	cis	Esophagus Mucosa	GTEx
rs11204743	GOLPH3L	cis	Nerve Tibial	GTEx
rs11204743	HORMAD1	cis	Adipose Subcutaneous	GTEx
rs11204743	CTSS	cis	Artery Tibial	GTEx
rs11204743	RP11-316M1.12	cis	Esophagus Muscularis	GTEx
rs11204743	RP11-316M1.12	cis	Artery Aorta	GTEx
rs11204743	CTSK	Cis_1M	lymphoblastoid	RTeQTL
rs11204743	RP11-316M1.12	cis	Esophagus Mucosa	GTEx
rs11204743	CTSS	Cis_1M	lymphoblastoid	RTeQTL
rs11204743	RP11-316M1.12	cis	Skin Sun Exposed Lower leg	GTEx
rs11204743	RP11-316M1.12	cis	Artery Tibial	GTEx
rs11204743	RP11-316M1.12	cis	Nerve Tibial	GTEx
rs11204743	GOLPH3L	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150879200-150898200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:150888000-150894800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr1:150890400-150890600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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