Variant report

Variant	rs1205099
Chromosome Location	chr14:72273652-72273653
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1204965	1.00[EUR][1000 genomes]
rs1204968	1.00[EUR][1000 genomes]
rs1209561	0.81[AFR][1000 genomes]
rs1212575	1.00[EUR][1000 genomes]
rs1892561	1.00[EUR][1000 genomes]
rs2096449	1.00[EUR][1000 genomes]
rs2802574	1.00[EUR][1000 genomes]
rs2802575	1.00[EUR][1000 genomes]
rs8013823	0.81[AFR][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	esv3398985	chr14:71927884-72404676	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1047559	chr14:72151736-72282151	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1342	chr14:72260578-72305563	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72271600-72274000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr14:72272000-72273800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr14:72272800-72274000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr14:72273400-72274000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr14:72273400-72274000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:72273400-72274200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr14:72273600-72273800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr14:72273600-72273800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr14:72273600-72274000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:72273600-72274000	Enhancers	Lung	lung

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