Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1000413	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10128809	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10506215	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10785374	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10785375	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10785376	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10880360	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11181669	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12425497	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12578732	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12816928	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12830101	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1914489	0.92[AFR][1000 genomes]
rs2056195	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2730983	0.89[AFR][1000 genomes]
rs3921403	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4768445	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4768446	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4768447	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7310956	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[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	nsv1044790	chr12:42672255-43344184	Enhancers Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
2	nsv541483	chr12:42672255-43344184	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
3	nsv832389	chr12:43003361-43173896	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43119600-43130000	Weak transcription	Esophagus	oesophagus
2	chr12:43123800-43128800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr12:43124200-43129200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:43124200-43129600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:43124400-43128800	Weak transcription	Colon Smooth Muscle	Colon
6	chr12:43124400-43129400	Weak transcription	Fetal Stomach	stomach
7	chr12:43124400-43129800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:43124600-43129800	Weak transcription	HMEC	breast
9	chr12:43127000-43128200	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr12:43127000-43131800	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr12:43127200-43130200	Enhancers	Fetal Heart	heart
12	chr12:43127400-43128000	Weak transcription	Left Ventricle	heart
13	chr12:43127400-43128400	Weak transcription	Right Atrium	heart
14	chr12:43127400-43129600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr12:43127400-43129800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr12:43127400-43129800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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