Variant report

Variant	rs4253217
Chromosome Location	chr10:50670590-50670591
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10776574	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11101148	0.98[EUR][1000 genomes]
rs12220258	0.80[ASN][1000 genomes]
rs1924489	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2209281	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2377938	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2889791	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3763730	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4240505	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4240506	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4253009	0.83[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4253226	0.80[ASN][1000 genomes]
rs4838516	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4838518	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4838519	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7070896	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7082895	0.84[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs7096755	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs7100734	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7899981	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7904860	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7906303	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7907557	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7908359	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7922756	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7923874	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs932735	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv895377	chr10:50588990-50678212	ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv831867	chr10:50607857-50788751	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	esv3346476	chr10:50610853-50987802	Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
6	esv3385048	chr10:50610942-50988537	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50656600-50672600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:50660400-50672400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:50662200-50677800	Weak transcription	Fetal Heart	heart
4	chr10:50662200-50691600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:50662400-50690000	Weak transcription	Stomach Mucosa	stomach
6	chr10:50662400-50693200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr10:50662600-50674800	Weak transcription	Colonic Mucosa	Colon
8	chr10:50662600-50676600	Weak transcription	Small Intestine	intestine
9	chr10:50662600-50677600	Weak transcription	NHDF-Ad	bronchial
10	chr10:50662600-50691400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr10:50663000-50675800	Weak transcription	Colon Smooth Muscle	Colon
12	chr10:50663200-50672600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr10:50663200-50693800	Weak transcription	HepG2	liver
14	chr10:50663400-50671200	Strong transcription	HMEC	breast
15	chr10:50663600-50671000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr10:50663600-50671000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:50663800-50671600	Weak transcription	Dnd41	blood
18	chr10:50663800-50672600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr10:50664000-50677400	Weak transcription	Fetal Kidney	kidney
20	chr10:50664600-50678200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr10:50665400-50671000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr10:50665600-50671600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr10:50665800-50672000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr10:50666200-50672600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:50666200-50674200	Weak transcription	Fetal Brain Male	brain
26	chr10:50666600-50676400	Weak transcription	K562	blood
27	chr10:50666600-50684400	Weak transcription	NHLF	lung
28	chr10:50666800-50678200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr10:50667200-50672000	Weak transcription	Thymus	Thymus
30	chr10:50667600-50672600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr10:50667600-50675600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr10:50667800-50671800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:50667800-50677600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr10:50667800-50707400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr10:50668000-50713400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr10:50668200-50674400	Weak transcription	Fetal Lung	lung
37	chr10:50668200-50675800	Weak transcription	Esophagus	oesophagus
38	chr10:50668200-50680200	Weak transcription	GM12878-XiMat	blood
39	chr10:50668400-50676400	Weak transcription	Hela-S3	cervix
40	chr10:50668400-50677600	Weak transcription	NH-A	brain
41	chr10:50668400-50677800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr10:50668400-50677800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr10:50668400-50678200	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr10:50668600-50672400	Weak transcription	Brain Germinal Matrix	brain
45	chr10:50668600-50674800	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr10:50668800-50677600	Weak transcription	Psoas Muscle	Psoas
47	chr10:50668800-50677800	Weak transcription	Fetal Thymus	thymus
48	chr10:50669000-50678200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr10:50669200-50671600	Weak transcription	Primary hematopoietic stem cells	blood
50	chr10:50669400-50671800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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