Variant report

Variant	rs71411760
Chromosome Location	chr14:25400429-25400430
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:37)

rs_ID	r²[population]
rs10132498	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10136888	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10145291	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10150527	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10150946	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10162292	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10162405	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10162420	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10162424	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10162457	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10162461	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12101204	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12232232	0.90[ASN][1000 genomes]
rs12886877	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17109333	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1957764	0.90[ASN][1000 genomes]
rs28416145	0.89[ASN][1000 genomes]
rs28430842	0.93[ASN][1000 genomes]
rs28544091	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34298539	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35669399	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36053777	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4983036	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6650491	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6650513	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6650514	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6650515	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9285592	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9323571	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9323572	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9323573	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9323574	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9323575	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9323576	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs964109	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9783658	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9989227	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041336	chr14:24726564-25527319	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542000	chr14:24726564-25527319	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv901504	chr14:25184210-25646203	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv901508	chr14:25365505-25451903	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1041051	chr14:25388230-25480511	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1047792	chr14:25388933-25503799	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv901509	chr14:25398571-25743484	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25390200-25405200	Weak transcription	Pancreas	Pancrea
2	chr14:25391800-25403600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr14:25394800-25410400	Weak transcription	Fetal Muscle Leg	muscle
4	chr14:25395400-25410400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr14:25396600-25409200	Weak transcription	Left Ventricle	heart
6	chr14:25396600-25415800	Weak transcription	Fetal Brain Male	brain
7	chr14:25397800-25403600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:25397800-25403600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr14:25398000-25400800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr14:25398000-25407800	Weak transcription	HSMMtube	muscle
11	chr14:25398200-25403600	Weak transcription	Colon Smooth Muscle	Colon
12	chr14:25398200-25409400	Weak transcription	Fetal Lung	lung
13	chr14:25398400-25408600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr14:25398600-25405000	Weak transcription	HepG2	liver
15	chr14:25399000-25400600	Weak transcription	Small Intestine	intestine
16	chr14:25399000-25410600	Weak transcription	Fetal Intestine Small	intestine
17	chr14:25399200-25405200	Weak transcription	Right Ventricle	heart
18	chr14:25399400-25403400	Weak transcription	Brain Substantia Nigra	brain
19	chr14:25399400-25404400	Weak transcription	Brain Angular Gyrus	brain
20	chr14:25399400-25404600	Weak transcription	Brain Hippocampus Middle	brain
21	chr14:25399400-25404800	Weak transcription	Brain Anterior Caudate	brain
22	chr14:25399400-25405000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr14:25399400-25413800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr14:25399800-25403400	Weak transcription	Fetal Heart	heart
25	chr14:25399800-25413400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr14:25399800-25413600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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