Variant report

Variant	rs1886054
Chromosome Location	chr14:25441887-25441888
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10139814	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17185509	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17185593	0.92[JPT][hapmap]
rs17257752	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs56362631	0.81[AFR][1000 genomes]
rs58764839	0.99[ASN][1000 genomes]
rs59366121	0.99[ASN][1000 genomes]
rs59957224	0.98[ASN][1000 genomes]
rs60667968	0.98[ASN][1000 genomes]
rs60783613	0.85[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:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25424600-25460600	Weak transcription	Fetal Muscle Trunk	muscle
2	chr14:25430000-25465800	Weak transcription	Lung	lung
3	chr14:25435800-25443600	Weak transcription	Right Atrium	heart
4	chr14:25435800-25443800	Weak transcription	Fetal Brain Female	brain
5	chr14:25435800-25447400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr14:25436000-25443400	Weak transcription	Fetal Lung	lung
7	chr14:25436200-25443200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr14:25436200-25447000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr14:25436200-25448000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr14:25436200-25451200	Weak transcription	A549	lung
11	chr14:25436400-25443400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr14:25436400-25443400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr14:25436400-25443600	Weak transcription	Left Ventricle	heart
14	chr14:25436600-25454200	Weak transcription	Fetal Muscle Leg	muscle
15	chr14:25436600-25454400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:25436600-25455400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:25436800-25442000	Weak transcription	Pancreas	Pancrea
18	chr14:25436800-25451200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr14:25437200-25448000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr14:25438200-25448000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr14:25440600-25442000	Enhancers	Fetal Intestine Large	intestine
22	chr14:25440600-25442000	Enhancers	Fetal Intestine Small	intestine
23	chr14:25441000-25443200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr14:25441000-25454200	Weak transcription	Fetal Brain Male	brain
25	chr14:25441200-25443200	Weak transcription	Colon Smooth Muscle	Colon
26	chr14:25441400-25442000	Enhancers	HepG2	liver
27	chr14:25441400-25443800	Strong transcription	HSMM	muscle
28	chr14:25441400-25445000	Weak transcription	Brain Angular Gyrus	brain
29	chr14:25441600-25444400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr14:25441600-25445000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr14:25441800-25442200	Weak transcription	Brain Hippocampus Middle	brain
32	chr14:25441800-25443000	Weak transcription	Fetal Heart	heart
33	chr14:25441800-25444400	Weak transcription	Brain Anterior Caudate	brain

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