Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10746996	0.89[ASN][1000 genomes]
rs10746997	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10781346	0.85[ASN][1000 genomes]
rs10781348	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10781349	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10781352	0.90[EUR][1000 genomes]
rs10869736	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10869737	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10869740	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11144801	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1125312	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12336492	0.87[ASN][1000 genomes]
rs1495255	0.83[ASN][1000 genomes]
rs3913046	0.86[ASN][1000 genomes]
rs4545165	0.81[ASN][1000 genomes]
rs4745528	0.83[ASN][1000 genomes]
rs4745529	0.91[EUR][1000 genomes]
rs60800515	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6560508	0.87[ASN][1000 genomes]
rs7033364	0.85[ASN][1000 genomes]
rs7853361	0.89[EUR][1000 genomes]
rs7854188	0.83[ASN][1000 genomes]
rs952503	0.89[ASN][1000 genomes]
rs990559	0.85[ASN][1000 genomes]
rs990560	0.83[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	nsv869152	chr9:78742197-79583399	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv893476	chr9:78768830-78887992	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:78814000-78848200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr9:78830800-78842400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:78834800-78840600	Weak transcription	Fetal Intestine Small	intestine
4	chr9:78835000-78840400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr9:78837000-78840600	Weak transcription	Fetal Intestine Large	intestine
6	chr9:78838800-78841000	Enhancers	Placenta	Placenta
7	chr9:78839600-78853800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr9:78840200-78840600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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