Variant report

Variant	rs10810629
Chromosome Location	chr9:16787786-16787787
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10756811	0.81[CEU][hapmap];0.86[AMR][1000 genomes]
rs10756812	1.00[CEU][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10810616	0.81[CEU][hapmap];0.88[AMR][1000 genomes]
rs10810619	0.81[CEU][hapmap];0.88[AMR][1000 genomes]
rs10810628	1.00[CEU][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10962570	0.84[CEU][hapmap];0.92[AMR][1000 genomes]
rs10962572	0.87[AMR][1000 genomes]
rs10962573	0.88[AMR][1000 genomes]
rs10962582	0.85[CEU][hapmap]
rs10962585	0.86[AMR][1000 genomes]
rs10962590	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11793056	0.88[AMR][1000 genomes]
rs11793537	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11795031	0.90[CEU][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12343424	0.89[AMR][1000 genomes]
rs12344347	0.82[CEU][hapmap];0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12344799	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12353453	0.82[CEU][hapmap];0.89[AMR][1000 genomes]
rs13294647	0.82[CEU][hapmap];0.92[AMR][1000 genomes]
rs13299347	0.81[AMR][1000 genomes]
rs1330299	0.81[AMR][1000 genomes]
rs4623533	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs56343038	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs944207	0.82[CEU][hapmap];0.90[AMR][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	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	esv2758627	chr9:16641966-16809203	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2759673	chr9:16641966-16809203	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv892650	chr9:16696187-16950860	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16767600-16795400	Weak transcription	Fetal Muscle Leg	muscle
2	chr9:16768000-16795000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:16769800-16795400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:16773000-16795000	Weak transcription	HSMMtube	muscle
5	chr9:16784400-16802200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:16785000-16792200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr9:16785200-16794600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr9:16786000-16795600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:16786600-16788000	Strong transcription	Fetal Stomach	stomach
10	chr9:16786600-16788200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr9:16787000-16788000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:16787000-16788200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr9:16787000-16792400	Weak transcription	Colon Smooth Muscle	Colon
14	chr9:16787000-16794600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr9:16787000-16795200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr9:16787200-16787800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:16787200-16788200	Enhancers	NHDF-Ad	bronchial
18	chr9:16787200-16794800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr9:16787200-16797600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:16787400-16788000	Enhancers	NH-A	brain
21	chr9:16787400-16788200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr9:16787400-16788200	Genic enhancers	HSMM	muscle
23	chr9:16787400-16788200	Enhancers	HUVEC	blood vessel
24	chr9:16787400-16788200	Enhancers	Osteobl	bone
25	chr9:16787400-16788400	Strong transcription	Ovary	ovary
26	chr9:16787600-16787800	Weak transcription	NHLF	lung
27	chr9:16787600-16788000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:16787600-16788200	Enhancers	Muscle Satellite Cultured Cells	--
29	chr9:16787600-16788200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:16787600-16788200	Strong transcription	Stomach Smooth Muscle	stomach
31	chr9:16787600-16792200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:16787600-16792600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr9:16787600-16795000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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