Variant report

Variant	rs10996458
Chromosome Location	chr10:53027701-53027702
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10490973	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490974	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490975	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996310	0.94[EUR][1000 genomes]
rs10996313	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996314	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996317	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996318	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996319	0.92[EUR][1000 genomes]
rs10996322	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996323	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996325	0.96[EUR][1000 genomes]
rs10996327	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996328	0.96[EUR][1000 genomes]
rs10996331	0.96[EUR][1000 genomes]
rs10996357	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996361	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996373	1.00[ASN][1000 genomes]
rs10996376	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996377	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996389	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996390	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996392	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996397	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996427	0.98[AFR][1000 genomes]
rs10996438	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996449	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10996452	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10996455	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12240684	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12245444	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12247775	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12251510	0.96[EUR][1000 genomes]
rs12253079	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12253122	0.96[EUR][1000 genomes]
rs12254957	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12259761	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12262817	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12264019	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16915897	0.96[EUR][1000 genomes]
rs61849755	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61849756	0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61849757	0.86[AMR][1000 genomes]
rs61849758	0.83[AMR][1000 genomes]
rs61852060	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7085957	0.83[AMR][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	nsv1036645	chr10:52804961-53159076	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv831874	chr10:53010357-53195508	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 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	chr10:53018400-53051200	Weak transcription	Aorta	Aorta
2	chr10:53021200-53028400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr10:53022800-53028400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr10:53025400-53028400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr10:53025400-53030000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr10:53026000-53028400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr10:53026200-53030800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr10:53026400-53029000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr10:53026600-53028400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr10:53026600-53029800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:53026600-53041800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr10:53026800-53029400	Weak transcription	NHDF-Ad	bronchial
13	chr10:53027000-53028600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:53027000-53029200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:53027000-53032400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr10:53027600-53028200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr10:53027600-53028400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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