Variant report

Variant	rs72712549
Chromosome Location	chr14:63680404-63680405
allele	G/T
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:11)

rs_ID	r²[population]
rs17093475	1.00[ASN][1000 genomes]
rs17100865	1.00[ASN][1000 genomes]
rs55892114	1.00[ASN][1000 genomes]
rs56871823	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs58187111	1.00[ASN][1000 genomes]
rs58799281	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs66514279	1.00[ASN][1000 genomes]
rs67466036	1.00[ASN][1000 genomes]
rs7145437	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72712550	1.00[ASN][1000 genomes]
rs72712551	0.95[AFR][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	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv564893	chr14:63526931-63796122	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1045599	chr14:63540073-63765152	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv530774	chr14:63591348-64029881	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63672000-63717000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:63672200-63681400	Weak transcription	Lung	lung
3	chr14:63672200-63683400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr14:63673000-63681200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr14:63673000-63682600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr14:63673200-63681400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr14:63673400-63691000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr14:63673600-63689800	Weak transcription	Colon Smooth Muscle	Colon
9	chr14:63674600-63681400	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr14:63675800-63680800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:63675800-63686000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:63676200-63680600	Weak transcription	Ovary	ovary
13	chr14:63676200-63683000	Strong transcription	Cortex derived primary cultured neurospheres	brain
14	chr14:63676200-63707600	Weak transcription	Aorta	Aorta
15	chr14:63676400-63683600	Genic enhancers	HUVEC	blood vessel
16	chr14:63676400-63733600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr14:63677000-63680800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr14:63677400-63681200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr14:63678200-63681000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr14:63678600-63680600	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr14:63678600-63680800	Strong transcription	Fetal Lung	lung
22	chr14:63679200-63681200	Weak transcription	Adipose Nuclei	Adipose
23	chr14:63679400-63717000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr14:63679800-63684600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr14:63680000-63680600	ZNF genes & repeats	Fetal Muscle Leg	muscle
26	chr14:63680000-63689600	Weak transcription	NH-A	brain
27	chr14:63680200-63681200	Weak transcription	Left Ventricle	heart
28	chr14:63680400-63680600	Strong transcription	Stomach Smooth Muscle	stomach
29	chr14:63680400-63681200	Strong transcription	Fetal Stomach	stomach
30	chr14:63680400-63681600	Enhancers	Right Atrium	heart

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