Variant report

Variant	rs9971367
Chromosome Location	chr10:21579841-21579842
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10218879	0.89[ASN][1000 genomes]
rs10218952	0.89[ASN][1000 genomes]
rs10218971	0.89[ASN][1000 genomes]
rs10218986	0.89[ASN][1000 genomes]
rs11012642	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012644	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012645	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012646	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012648	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012651	0.81[AMR][1000 genomes]
rs11012658	1.00[ASN][1000 genomes]
rs11012665	0.89[ASN][1000 genomes]
rs12240956	1.00[ASN][1000 genomes]
rs12248522	0.89[ASN][1000 genomes]
rs12250778	0.89[ASN][1000 genomes]
rs12256314	0.89[ASN][1000 genomes]
rs12359942	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13377089	1.00[ASN][1000 genomes]
rs16921726	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16921744	0.89[ASN][1000 genomes]
rs2360046	0.89[ASN][1000 genomes]
rs28476641	1.00[ASN][1000 genomes]
rs34299719	0.89[ASN][1000 genomes]
rs55638725	1.00[ASN][1000 genomes]
rs55672286	1.00[ASN][1000 genomes]
rs60875963	1.00[ASN][1000 genomes]
rs61851539	0.89[ASN][1000 genomes]
rs61851542	0.89[ASN][1000 genomes]
rs7080191	0.89[ASN][1000 genomes]
rs7085637	1.00[ASN][1000 genomes]
rs7090939	0.89[ASN][1000 genomes]
rs7091420	0.89[ASN][1000 genomes]
rs7894995	0.89[ASN][1000 genomes]
rs7900321	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7907491	0.89[ASN][1000 genomes]
rs7910000	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7913116	0.89[ASN][1000 genomes]
rs7922927	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9971139	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9971348	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv971871	chr10:21460392-21579987	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv831807	chr10:21509185-21688043	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2761579	chr10:21554557-21612760	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21564200-21581600	Weak transcription	Right Atrium	heart
2	chr10:21567400-21582800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:21568200-21580400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr10:21568200-21581600	Weak transcription	Ovary	ovary
5	chr10:21570200-21580400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr10:21571600-21583000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:21575000-21581000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr10:21575000-21581800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr10:21575200-21580000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr10:21576400-21581800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr10:21576400-21583200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:21578200-21580000	Genic enhancers	A549	lung
13	chr10:21578200-21580600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr10:21578200-21580600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr10:21578400-21581800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr10:21578600-21580000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr10:21578600-21580800	Weak transcription	Adipose Nuclei	Adipose
18	chr10:21578600-21580800	Weak transcription	Fetal Lung	lung
19	chr10:21578800-21580000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr10:21578800-21580800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:21579000-21580200	Enhancers	HSMMtube	muscle
22	chr10:21579000-21580400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr10:21579000-21581000	Enhancers	NHDF-Ad	bronchial
24	chr10:21579200-21580000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr10:21579200-21580600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:21579200-21580800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr10:21579200-21580800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:21579200-21580800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr10:21579400-21580000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr10:21579400-21580800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr10:21579400-21581000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr10:21579400-21582600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr10:21579600-21580000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr10:21579600-21580200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr10:21579600-21580600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr10:21579800-21580000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr10:21579800-21580000	Enhancers	Fetal Muscle Leg	muscle
38	chr10:21579800-21580000	Weak transcription	NHLF	lung
39	chr10:21579800-21580400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr10:21579800-21581000	Enhancers	Osteobl	bone

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