Variant report

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

rs_ID	r²[population]
rs10516038	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11738000	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11750131	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12651802	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12657288	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13436455	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1834118	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2018599	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2336972	0.83[AMR][1000 genomes]
rs2337000	0.84[EUR][1000 genomes]
rs2973664	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4479863	0.93[EUR][1000 genomes]
rs4583906	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4624810	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61165988	0.95[EUR][1000 genomes]
rs6861976	0.80[EUR][1000 genomes]
rs6862936	0.95[EUR][1000 genomes]
rs6879227	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6891311	0.93[EUR][1000 genomes]
rs7703401	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[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	nsv932627	chr5:166744408-167290959	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1032559	chr5:167070888-167210684	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1027805	chr5:167082800-167285008	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167152600-167170000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:167157800-167170200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:167158000-167170000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:167158000-167170000	Weak transcription	NH-A	brain
5	chr5:167158000-167170600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr5:167158800-167170800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr5:167159200-167171000	Weak transcription	HSMM	muscle
8	chr5:167164000-167166600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr5:167164800-167169800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:167165200-167166600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:167165200-167170800	Weak transcription	Fetal Lung	lung
12	chr5:167166000-167166800	Weak transcription	Cortex derived primary cultured neurospheres	brain

Quick Search: