Variant report

Variant	rs74045753
Chromosome Location	chr14:38371222-38371223
allele	A/G
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:17)

rs_ID	r²[population]
rs56120250	1.00[AMR][1000 genomes]
rs59375635	1.00[AMR][1000 genomes]
rs60265164	1.00[AMR][1000 genomes]
rs74045692	1.00[AMR][1000 genomes]
rs74045694	1.00[AMR][1000 genomes]
rs74045695	1.00[AMR][1000 genomes]
rs74045702	1.00[AMR][1000 genomes]
rs74045723	0.80[AFR][1000 genomes]
rs74045751	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74045771	1.00[AMR][1000 genomes]
rs74045773	1.00[AMR][1000 genomes]
rs74045774	1.00[AMR][1000 genomes]
rs74045775	1.00[AMR][1000 genomes]
rs74045783	1.00[AMR][1000 genomes]
rs74045789	1.00[AMR][1000 genomes]
rs74045790	1.00[AMR][1000 genomes]
rs74048803	1.00[AMR][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	nsv916985	chr14:38052347-38838551	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
2	nsv1051120	chr14:38294270-38436127	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv542046	chr14:38294270-38436127	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv564387	chr14:38357864-38563111	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3354861	chr14:38359630-38392369	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv994902	chr14:38368430-38374964	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38365000-38372600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr14:38369600-38371600	Enhancers	Fetal Lung	lung
3	chr14:38370000-38371400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:38370200-38371600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr14:38370200-38371800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr14:38370200-38372200	Flanking Active TSS	NHDF-Ad	bronchial
7	chr14:38370400-38371600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr14:38370800-38372200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr14:38371000-38371400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr14:38371000-38371400	Flanking Active TSS	Osteobl	bone
11	chr14:38371000-38371600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr14:38371200-38371400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:38371200-38371400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr14:38371200-38371400	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
15	chr14:38371200-38371400	Enhancers	NHLF	lung
16	chr14:38371200-38371600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr14:38371200-38371600	Enhancers	Hela-S3	cervix
18	chr14:38371200-38371800	Enhancers	NH-A	brain

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