Variant report

Variant	rs58075729
Chromosome Location	chr4:26842824-26842825
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:26837390..26839392-chr4:26842052..26843597,2	K562	blood:
2	chr4:26842658..26844701-chr4:26856805..26859356,2	K562	blood:
3	chr4:26840051..26842840-chr4:26845886..26847935,2	K562	blood:

Variant related genes	Relation type
ENSG00000109689	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10029307	0.81[ASN][1000 genomes]
rs11729927	0.80[ASN][1000 genomes]
rs11730235	0.80[ASN][1000 genomes]
rs11737218	0.87[ASN][1000 genomes]
rs11943948	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12641261	0.87[ASN][1000 genomes]
rs12644073	0.82[ASN][1000 genomes]
rs12646473	0.86[ASN][1000 genomes]
rs12650172	0.87[ASN][1000 genomes]
rs13116341	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13138942	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13139464	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28497454	0.80[ASN][1000 genomes]
rs34996346	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3924178	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4274829	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4407490	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4505809	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4519790	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4532223	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4557250	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4557251	0.89[ASN][1000 genomes]
rs58968032	0.85[ASN][1000 genomes]
rs6448479	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6448484	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6815719	0.87[ASN][1000 genomes]
rs6833053	0.87[ASN][1000 genomes]
rs6833895	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6853032	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73811400	0.87[ASN][1000 genomes]
rs73813220	0.81[ASN][1000 genomes]
rs7655686	0.82[ASN][1000 genomes]
rs9790789	0.84[AMR][1000 genomes];0.83[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	nsv470021	chr4:26721578-27067027	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1001306	chr4:26821511-26955344	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs58075729	STIM2	Cis_1M	lymphoblastoid	RTeQTL
rs58075729	RP11-293A21.1	cis	Thyroid	GTEx
rs58075729	RP11-293A21.1	cis	Skin Sun Exposed Lower leg	GTEx
rs58075729	RP11-293A21.1	cis	Adipose Subcutaneous	GTEx
rs58075729	RP11-293A21.1	cis	lung	GTEx

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26839200-26843200	Enhancers	Fetal Heart	heart
2	chr4:26840000-26858800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:26840600-26844200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr4:26841200-26843400	Enhancers	Thymus	Thymus
5	chr4:26841400-26845400	Weak transcription	Gastric	stomach
6	chr4:26841400-26858600	Weak transcription	Aorta	Aorta
7	chr4:26841600-26843600	Weak transcription	Right Atrium	heart
8	chr4:26841600-26858600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:26842200-26843400	Enhancers	Fetal Thymus	thymus
10	chr4:26842400-26858800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:26842800-26845800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:26842800-26846400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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