Variant report

Variant	rs10509599
Chromosome Location	chr10:92074146-92074147
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10881777	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10881778	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10881779	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10881780	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10881781	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11186105	0.80[EUR][1000 genomes]
rs11186108	0.90[EUR][1000 genomes]
rs11186109	0.88[EUR][1000 genomes]
rs11186110	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11186113	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11186118	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11186119	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11186120	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12355886	1.00[ASN][1000 genomes]
rs12357905	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12359346	0.91[EUR][1000 genomes]
rs12762427	0.86[ASN][1000 genomes]
rs12778222	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12778519	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12782505	1.00[ASN][1000 genomes]
rs12784906	1.00[ASN][1000 genomes]
rs12785026	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1409299	0.84[EUR][1000 genomes]
rs1570990	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1570991	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1926100	0.88[EUR][1000 genomes]
rs2182383	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2419663	0.86[AFR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2419664	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2419665	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2900954	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2900955	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35835425	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3981442	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4253986	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6583699	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7072968	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7075606	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7089493	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7093547	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7475887	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7905612	0.85[EUR][1000 genomes]
rs9732926	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9733097	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9733896	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895883	chr10:91610601-92195828	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1039731	chr10:91645718-92198264	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv540743	chr10:91645718-92198264	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv467430	chr10:91681344-92297943	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv551875	chr10:91681344-92297943	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	esv3375393	chr10:91880933-92243227	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv2422237	chr10:91940542-92547558	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1037720	chr10:92063438-92259359	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:92061400-92077800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr10:92063800-92074200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr10:92065600-92074200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr10:92069600-92077000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr10:92072800-92074600	Enhancers	Placenta Amnion	Placenta Amnion
6	chr10:92073000-92074800	Enhancers	HMEC	breast
7	chr10:92073000-92076800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr10:92073000-92077200	Enhancers	HUVEC	blood vessel
9	chr10:92073200-92074600	Enhancers	Hela-S3	cervix
10	chr10:92073200-92074800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr10:92073200-92074800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr10:92073200-92074800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr10:92073400-92074200	Enhancers	NHDF-Ad	bronchial
14	chr10:92073400-92074600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:92073400-92074600	Enhancers	NH-A	brain
16	chr10:92073400-92074800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr10:92073400-92074800	Enhancers	NHLF	lung
18	chr10:92073400-92074800	Enhancers	Osteobl	bone
19	chr10:92073600-92074400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr10:92073600-92077800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr10:92073800-92074600	Enhancers	Fetal Intestine Large	intestine
22	chr10:92073800-92078800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr10:92074000-92074400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr10:92074000-92074400	Enhancers	Brain Germinal Matrix	brain
25	chr10:92074000-92074400	Enhancers	HSMM	muscle
26	chr10:92074000-92074600	Flanking Active TSS	NHEK	skin
27	chr10:92074000-92074800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr10:92074000-92075800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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