Variant report

Variant	rs2015463
Chromosome Location	chr14:37239386-37239387
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1325541	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1631933	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1652247	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1652275	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1749935	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1806899	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2415363	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7144852	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7154494	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs730643	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8008462	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs912814	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[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	nsv1047290	chr14:36564568-37445157	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
2	nsv1037952	chr14:36670484-37294692	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv542042	chr14:36670484-37294692	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	nsv1053685	chr14:36915643-37245920	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37237400-37240600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr14:37237800-37241200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr14:37238000-37242000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr14:37238000-37242000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr14:37238000-37242400	Weak transcription	HMEC	breast
6	chr14:37238000-37242600	Weak transcription	NHEK	skin
7	chr14:37238000-37243000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:37238200-37243000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:37238400-37240600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:37238400-37240600	Weak transcription	Esophagus	oesophagus
11	chr14:37238400-37242200	Weak transcription	K562	blood
12	chr14:37238400-37242400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr14:37238400-37243000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr14:37239000-37240000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

Quick Search:

Input of quick search could be:

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

what's new

Quick links