Variant report

Variant	rs10816963
Chromosome Location	chr9:99811261-99811262
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10114720	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10118886	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10118923	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10123754	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10123757	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10739289	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10739296	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10759389	0.92[EUR][1000 genomes]
rs10759391	0.90[EUR][1000 genomes]
rs10759399	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10759400	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10759406	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10759417	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10759420	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10816926	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10816951	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10816953	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10816962	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10816964	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10816981	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10816984	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10816994	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10817013	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10980241	0.92[EUR][1000 genomes]
rs10980243	0.92[EUR][1000 genomes]
rs10980326	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10980346	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10980396	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12236690	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12376012	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12376575	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12377546	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13285842	0.82[ASN][1000 genomes]
rs15394	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16919034	0.88[EUR][1000 genomes]
rs16924211	0.83[ASN][1000 genomes]
rs2004336	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34342973	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4367680	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4501700	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4510972	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59995818	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62560873	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6477844	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7023974	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7035822	0.90[EUR][1000 genomes]
rs7038926	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7039198	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7857836	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7873286	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7875800	0.89[EUR][1000 genomes]
rs9792463	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[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	nsv1053215	chr9:99483926-99824810	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv428540	chr9:99722815-99863455	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv831662	chr9:99752521-99939231	Bivalent Enhancer Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99807800-99815000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:99808600-99814400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:99808800-99815000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:99809000-99813200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:99809000-99814400	Weak transcription	Fetal Intestine Large	intestine
6	chr9:99809200-99812800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr9:99809400-99812600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr9:99809400-99814400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr9:99809400-99814400	Weak transcription	Fetal Intestine Small	intestine
10	chr9:99809600-99813200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr9:99809800-99813200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:99810200-99813000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr9:99810200-99813000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr9:99810200-99814200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr9:99810200-99818400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr9:99811200-99811600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:99811200-99813200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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