Variant report

Variant	rs59300744
Chromosome Location	chr14:80015151-80015152
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10148779	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10467836	0.85[EUR][1000 genomes]
rs1364604	0.95[ASN][1000 genomes]
rs1364606	0.95[ASN][1000 genomes]
rs1544726	0.95[ASN][1000 genomes]
rs1544842	0.87[ASN][1000 genomes]
rs17109451	0.85[EUR][1000 genomes]
rs17764137	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59093010	0.85[EUR][1000 genomes]
rs7141526	0.95[ASN][1000 genomes]
rs7145283	0.85[EUR][1000 genomes]
rs7148240	0.95[ASN][1000 genomes]
rs7154918	0.93[ASN][1000 genomes]
rs7156216	0.93[ASN][1000 genomes]
rs7157577	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7160334	0.93[ASN][1000 genomes]
rs73326050	0.95[ASN][1000 genomes]
rs9323674	0.95[ASN][1000 genomes]
rs9652379	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv902112	chr14:79939393-80050771	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv869542	chr14:80009619-80118315	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:80009600-80018000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr14:80010400-80015800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr14:80010400-80018000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:80010800-80019000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr14:80011000-80018800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr14:80011600-80015800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr14:80011800-80015200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr14:80011800-80015600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr14:80011800-80069200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr14:80012000-80015200	Weak transcription	Osteobl	bone
11	chr14:80012000-80015600	Weak transcription	NH-A	brain
12	chr14:80013000-80015600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr14:80013600-80015800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:80014400-80037800	Weak transcription	Aorta	Aorta
15	chr14:80015000-80016000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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