Variant report

Variant	rs10965054
Chromosome Location	chr9:21534477-21534478
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10491567	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10811549	0.89[EUR][1000 genomes]
rs10811551	0.87[EUR][1000 genomes]
rs10811556	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10811557	0.87[AMR][1000 genomes]
rs10811562	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10811563	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10811564	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10811565	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10811566	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10811568	0.93[ASN][1000 genomes]
rs10965019	0.82[EUR][1000 genomes]
rs10965024	0.82[EUR][1000 genomes]
rs10965031	0.87[EUR][1000 genomes]
rs10965034	0.82[EUR][1000 genomes]
rs10965036	0.82[EUR][1000 genomes]
rs10965049	0.95[ASN][1000 genomes]
rs10965050	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10965053	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10965059	0.95[EUR][1000 genomes]
rs10965060	0.84[ASN][1000 genomes]
rs10965063	0.89[EUR][1000 genomes]
rs1125488	0.84[EUR][1000 genomes]
rs12375583	0.82[EUR][1000 genomes]
rs12377379	0.95[EUR][1000 genomes]
rs12378286	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12378990	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12379382	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12379709	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12379721	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1332188	0.82[EUR][1000 genomes]
rs16938433	0.82[EUR][1000 genomes]
rs16938435	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16938448	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2039380	0.85[EUR][1000 genomes]
rs55683539	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55835613	0.95[EUR][1000 genomes]
rs56122777	0.95[EUR][1000 genomes]
rs56337511	0.82[EUR][1000 genomes]
rs7026731	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7032680	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7041183	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72703410	0.80[EUR][1000 genomes]
rs72703411	0.87[EUR][1000 genomes]
rs72703417	0.82[EUR][1000 genomes]
rs72703418	0.82[EUR][1000 genomes]
rs72703419	0.82[EUR][1000 genomes]
rs72703426	0.82[EUR][1000 genomes]
rs72703442	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs72703445	0.95[EUR][1000 genomes]
rs72703447	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72703448	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs72703449	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72703450	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9644855	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892740	chr9:21471499-21551513	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA	110 gene(s)	inside rSNPs	diseases
2	nsv1031432	chr9:21472601-21608774	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases
3	nsv540085	chr9:21472601-21608774	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases
4	nsv892741	chr9:21517302-21551513	Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	esv3401423	chr9:21534096-21534645	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21507200-21551400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:21508000-21542000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:21516800-21542600	Weak transcription	Stomach Mucosa	stomach
4	chr9:21526400-21534800	Strong transcription	NHEK	skin
5	chr9:21526800-21534800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr9:21527800-21536600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:21528800-21535800	Weak transcription	Gastric	stomach
8	chr9:21528800-21542000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:21529000-21534800	Weak transcription	Esophagus	oesophagus
10	chr9:21529000-21551400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:21530800-21535000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr9:21531600-21542600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr9:21532200-21542800	Weak transcription	NHLF	lung
14	chr9:21532400-21534600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr9:21532400-21542000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:21533000-21535000	Weak transcription	Hela-S3	cervix
17	chr9:21533000-21535000	Strong transcription	Osteobl	bone
18	chr9:21533200-21534800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:21533200-21535000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr9:21533200-21535000	Weak transcription	NH-A	brain
21	chr9:21533200-21542600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr9:21533800-21535200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr9:21533800-21536000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr9:21534000-21535000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr9:21534000-21535000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:21534000-21535200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr9:21534000-21535200	Strong transcription	HMEC	breast
28	chr9:21534000-21535800	Strong transcription	A549	lung
29	chr9:21534000-21542000	Weak transcription	HUVEC	blood vessel
30	chr9:21534000-21543000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr9:21534000-21544200	Weak transcription	NHDF-Ad	bronchial
32	chr9:21534400-21548200	Weak transcription	HSMM	muscle

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