Variant report

Variant	rs58751289
Chromosome Location	chr11:102099123-102099124
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10895272	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10895273	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10895274	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10895275	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10895276	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10895277	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10895278	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10895280	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10895282	0.82[ASN][1000 genomes]
rs11225156	0.86[EUR][1000 genomes]
rs11225160	0.84[EUR][1000 genomes]
rs11225163	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11225165	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11225167	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11225170	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11225174	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11225177	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11605954	0.83[EUR][1000 genomes]
rs11608234	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12223991	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12226331	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12420287	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12421242	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12786272	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12787996	0.87[EUR][1000 genomes]
rs12790399	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12795624	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12807220	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17097475	0.81[ASN][1000 genomes]
rs17097547	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17097560	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1820455	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1893498	0.84[EUR][1000 genomes]
rs2187525	0.82[EUR][1000 genomes]
rs2282652	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3858420	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4447144	0.83[EUR][1000 genomes]
rs4475891	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4754041	0.83[EUR][1000 genomes]
rs57027482	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61280272	0.89[ASN][1000 genomes]
rs7110557	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7112802	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7120067	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7122907	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7124247	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs718891	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7931576	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7942061	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8504	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[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	esv3362945	chr11:101736547-102114246	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv1052348	chr11:101987090-102255753	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv556141	chr11:101988061-102207851	Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1050961	chr11:101993880-102253717	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv1051735	chr11:101993880-102255753	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv530646	chr11:102000840-102238992	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv832251	chr11:102012295-102181744	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv1043388	chr11:102017719-102172857	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102043800-102100400	Weak transcription	Pancreas	Pancrea
2	chr11:102059600-102100400	Weak transcription	Gastric	stomach
3	chr11:102064000-102105400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:102074000-102104200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:102075400-102105600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr11:102076200-102102200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:102078800-102105600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr11:102079000-102107200	Weak transcription	Fetal Brain Male	brain
9	chr11:102080800-102099600	Weak transcription	Colon Smooth Muscle	Colon
10	chr11:102081000-102100000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:102081200-102118600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr11:102086800-102111600	Weak transcription	Lung	lung
13	chr11:102088600-102105200	Weak transcription	Brain Substantia Nigra	brain
14	chr11:102091800-102102800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr11:102093000-102113000	Weak transcription	Ovary	ovary
16	chr11:102094200-102101200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:102094400-102101800	Strong transcription	Liver	Liver
18	chr11:102094400-102102000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:102095200-102099800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr11:102095200-102100000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr11:102095200-102105400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr11:102095200-102118600	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr11:102095800-102099400	Strong transcription	Fetal Intestine Small	intestine
24	chr11:102095800-102101000	Strong transcription	Fetal Muscle Trunk	muscle
25	chr11:102095800-102101200	Genic enhancers	HepG2	liver
26	chr11:102096400-102099600	Strong transcription	Fetal Stomach	stomach
27	chr11:102096400-102101000	Strong transcription	Fetal Muscle Leg	muscle
28	chr11:102096600-102099200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr11:102096600-102099600	Strong transcription	Fetal Intestine Large	intestine
30	chr11:102096800-102099400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr11:102096800-102114600	Weak transcription	Small Intestine	intestine
32	chr11:102097000-102100400	Weak transcription	Esophagus	oesophagus
33	chr11:102097000-102102000	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr11:102097000-102105800	Weak transcription	Right Ventricle	heart
35	chr11:102097200-102100400	Strong transcription	Placenta	Placenta
36	chr11:102097200-102105800	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr11:102097400-102105400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr11:102097600-102105200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:102097800-102099400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:102097800-102099600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr11:102097800-102100000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr11:102097800-102100400	Weak transcription	A549	lung
43	chr11:102097800-102100600	Weak transcription	Stomach Mucosa	stomach
44	chr11:102097800-102102600	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr11:102097800-102119600	Weak transcription	Right Atrium	heart
46	chr11:102098000-102099400	Weak transcription	HSMMtube	muscle
47	chr11:102098000-102099600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr11:102098000-102099600	Weak transcription	Fetal Heart	heart
49	chr11:102098000-102100200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr11:102098000-102100400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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