Variant report

Variant	rs361231
Chromosome Location	chr3:136716773-136716774
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs108858	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13095034	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1385306	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1654900	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1654901	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1682361	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1682362	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1682363	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1682364	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1682365	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1682366	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs181732	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2086880	0.85[EUR][1000 genomes]
rs2117008	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2344092	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34564994	0.80[EUR][1000 genomes]
rs361227	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs361228	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs361229	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs361232	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs361233	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs361234	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs361235	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4678278	0.86[EUR][1000 genomes]
rs55781515	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6439677	0.88[EUR][1000 genomes]
rs6766766	0.85[EUR][1000 genomes]
rs6766858	0.85[EUR][1000 genomes]
rs6802479	0.84[EUR][1000 genomes]
rs71620537	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs754694	0.86[EUR][1000 genomes]
rs7640951	0.83[EUR][1000 genomes]
rs7646307	0.85[EUR][1000 genomes]
rs835627	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs835628	0.85[EUR][1000 genomes]
rs835629	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs835630	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs835631	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs835651	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs835652	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs900947	0.86[EUR][1000 genomes]
rs900948	0.86[EUR][1000 genomes]
rs900949	0.86[EUR][1000 genomes]
rs900950	0.86[EUR][1000 genomes]
rs9681468	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9817061	0.82[EUR][1000 genomes]
rs9827066	0.86[EUR][1000 genomes]
rs9845076	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9850024	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9854795	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9874615	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9875855	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs999038	0.85[EUR][1000 genomes];0.82[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	nsv877534	chr3:136676303-136765859	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv524856	chr3:136693459-137190765	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1012111	chr3:136695367-137343430	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136703800-136732400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:136704000-136730600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:136704800-136731000	Weak transcription	HSMMtube	muscle
4	chr3:136708800-136720000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr3:136710000-136731000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:136713600-136732800	Weak transcription	Primary T cells from cord blood	blood
7	chr3:136714000-136730800	Weak transcription	HSMM	muscle
8	chr3:136714400-136730800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr3:136714800-136717400	Weak transcription	NHDF-Ad	bronchial
10	chr3:136715000-136729000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr3:136715200-136731000	Weak transcription	Adipose Nuclei	Adipose
12	chr3:136715200-136733000	Weak transcription	Left Ventricle	heart
13	chr3:136715400-136719400	Weak transcription	Esophagus	oesophagus
14	chr3:136715400-136730800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:136715600-136726000	Weak transcription	Fetal Thymus	thymus
16	chr3:136715600-136727000	Weak transcription	Thymus	Thymus
17	chr3:136715600-136730200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr3:136715800-136717400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr3:136715800-136717600	Weak transcription	Hela-S3	cervix
20	chr3:136715800-136719000	Weak transcription	HMEC	breast
21	chr3:136715800-136722800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr3:136715800-136730400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr3:136716000-136719000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr3:136716400-136718600	Weak transcription	NHEK	skin

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