Variant report

Variant	rs1951800
Chromosome Location	chr14:25397080-25397081
allele	A/G
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:38)

rs_ID	r²[population]
rs10483291	0.85[CEU][hapmap]
rs11159000	0.87[CEU][hapmap]
rs11159001	0.85[CEU][hapmap]
rs11847012	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1241598	0.93[CHB][hapmap]
rs12586327	0.85[CEU][hapmap]
rs12586425	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12588743	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12880456	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12880978	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12883258	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12885474	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12886704	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12887754	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12889054	0.98[ASN][1000 genomes]
rs12891857	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12893418	1.00[ASN][1000 genomes]
rs12896576	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17185369	0.93[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs17185376	0.93[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs17185397	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17185425	0.87[CEU][hapmap]
rs17257556	0.93[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs17257577	1.00[ASN][1000 genomes]
rs2038699	0.86[EUR][1000 genomes]
rs2877686	1.00[CEU][hapmap]
rs4561376	0.85[CEU][hapmap]
rs58423583	1.00[ASN][1000 genomes]
rs59153576	0.87[EUR][1000 genomes]
rs7141066	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs7154597	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7155229	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74040723	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs74040727	0.85[AFR][1000 genomes]
rs8003472	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs912306	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs912307	1.00[CEU][hapmap]
rs9671261	0.87[CEU][hapmap]

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	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

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25379400-25397800	Weak transcription	Right Ventricle	heart
2	chr14:25381400-25397800	Weak transcription	Fetal Intestine Small	intestine
3	chr14:25390200-25405200	Weak transcription	Pancreas	Pancrea
4	chr14:25391800-25397200	Weak transcription	HSMMtube	muscle
5	chr14:25391800-25403600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr14:25392000-25397200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr14:25393800-25397200	Enhancers	Brain Hippocampus Middle	brain
8	chr14:25394200-25397400	Enhancers	Fetal Heart	heart
9	chr14:25394600-25399400	Enhancers	Brain Angular Gyrus	brain
10	chr14:25394800-25410400	Weak transcription	Fetal Muscle Leg	muscle
11	chr14:25395400-25398000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr14:25395400-25410400	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr14:25395600-25399400	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr14:25395800-25397200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr14:25395800-25397400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr14:25395800-25398000	Weak transcription	HepG2	liver
17	chr14:25396400-25397200	Enhancers	Fetal Brain Female	brain
18	chr14:25396400-25397400	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr14:25396400-25397800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr14:25396400-25398200	Enhancers	Fetal Lung	lung
21	chr14:25396600-25397400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr14:25396600-25397800	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr14:25396600-25398400	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr14:25396600-25398400	Enhancers	HSMM	muscle
25	chr14:25396600-25399400	Enhancers	Brain Substantia Nigra	brain
26	chr14:25396600-25409200	Weak transcription	Left Ventricle	heart
27	chr14:25396600-25415800	Weak transcription	Fetal Brain Male	brain
28	chr14:25396800-25397600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr14:25396800-25397800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr14:25396800-25398000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr14:25396800-25398000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr14:25396800-25398400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:25396800-25399000	Enhancers	Small Intestine	intestine
34	chr14:25397000-25397400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr14:25397000-25397400	Enhancers	Brain Anterior Caudate	brain

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