Variant report

Variant	rs10458457
Chromosome Location	chr1:113966822-113966823
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11803682	0.83[ASN][1000 genomes]
rs17507414	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1936929	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2359416	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4839321	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4839322	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5023142	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61817538	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61819365	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6537789	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7518586	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7529062	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7551268	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[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	nsv427719	chr1:113570229-114078388	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv1010110	chr1:113856612-113969417	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
3	nsv1014757	chr1:113861524-113969417	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113940200-113987000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:113948000-113969800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:113949800-113972200	Weak transcription	Aorta	Aorta
4	chr1:113958400-113972200	Weak transcription	Ovary	ovary
5	chr1:113961200-113967800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:113961200-113971800	Weak transcription	Stomach Mucosa	stomach
7	chr1:113963600-113967600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:113964400-113967400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:113964400-113974200	Weak transcription	A549	lung
10	chr1:113964800-113968800	Weak transcription	Colon Smooth Muscle	Colon
11	chr1:113965200-113968000	Weak transcription	Primary T cells from cord blood	blood
12	chr1:113965200-113970000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:113965200-113970200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:113965200-113972200	Weak transcription	Left Ventricle	heart
15	chr1:113965400-113969800	Weak transcription	Gastric	stomach
16	chr1:113965800-113968200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:113965800-113969600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr1:113965800-113969800	Weak transcription	Pancreas	Pancrea
19	chr1:113966400-113972000	Weak transcription	Liver	Liver
20	chr1:113966800-113967200	Weak transcription	Esophagus	oesophagus
21	chr1:113966800-113967400	Weak transcription	Colonic Mucosa	Colon
22	chr1:113966800-113969200	Weak transcription	Fetal Stomach	stomach
23	chr1:113966800-113972000	Weak transcription	Lung	lung
24	chr1:113966800-113986600	Weak transcription	Fetal Intestine Small	intestine

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