Variant report

Variant	rs9818149
Chromosome Location	chr3:112841215-112841216
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10511318	0.81[AFR][1000 genomes]
rs10934216	0.83[ASN][1000 genomes]
rs10934217	0.83[ASN][1000 genomes]
rs1574478	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1797608	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1797621	0.82[ASN][1000 genomes]
rs1797622	0.82[ASN][1000 genomes]
rs2004990	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2017828	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2045687	0.82[ASN][1000 genomes]
rs2045688	0.82[ASN][1000 genomes]
rs2045690	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2045691	0.82[ASN][1000 genomes]
rs2613919	0.80[ASN][1000 genomes]
rs2613920	0.81[ASN][1000 genomes]
rs2613921	0.82[ASN][1000 genomes]
rs2613922	0.83[ASN][1000 genomes]
rs2613957	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2700202	0.83[ASN][1000 genomes]
rs2700204	0.80[ASN][1000 genomes]
rs2700205	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2700206	0.83[ASN][1000 genomes]
rs2700214	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2926811	0.82[ASN][1000 genomes]
rs2951458	0.82[ASN][1000 genomes]
rs2951459	0.82[ASN][1000 genomes]
rs2951460	0.82[ASN][1000 genomes]
rs2951461	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2951462	0.81[ASN][1000 genomes]
rs2951463	0.82[ASN][1000 genomes]
rs3852010	0.82[ASN][1000 genomes]
rs3852011	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4383482	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4387939	0.82[ASN][1000 genomes]
rs62262831	0.81[ASN][1000 genomes]
rs6438129	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6438130	0.83[ASN][1000 genomes]
rs6807101	0.83[ASN][1000 genomes]
rs7623035	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7632483	0.83[ASN][1000 genomes]
rs7650532	0.83[ASN][1000 genomes]
rs878460	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv877344	chr3:112789865-112854339	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv877345	chr3:112826253-112848851	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112837000-112842200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr3:112837600-112842800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:112837600-112842800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr3:112837600-112842800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr3:112840600-112846800	Weak transcription	Fetal Stomach	stomach

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