Variant report

Variant	rs59268439
Chromosome Location	chr14:25101897-25101898
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10138102	0.93[ASN][1000 genomes]
rs10149297	0.93[ASN][1000 genomes]
rs17257145	0.88[ASN][1000 genomes]
rs1957519	0.88[ASN][1000 genomes]
rs4981546	0.86[ASN][1000 genomes]
rs8192922	0.83[EUR][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	nsv1041336	chr14:24726564-25527319	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542000	chr14:24726564-25527319	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv510631	chr14:25045183-25172311	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv1843155	chr14:25099980-25110067	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25099400-25102200	Enhancers	Fetal Intestine Small	intestine
2	chr14:25099800-25102000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr14:25100200-25102600	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
4	chr14:25100800-25102000	Active TSS	Primary T cells fromperipheralblood	blood
5	chr14:25100800-25109600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:25101200-25103600	Enhancers	Fetal Thymus	thymus
7	chr14:25101200-25112800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr14:25101800-25102200	Enhancers	Fetal Muscle Leg	muscle
9	chr14:25101800-25102400	Enhancers	Fetal Intestine Large	intestine
10	chr14:25101800-25103400	Active TSS	Primary T helper cells PMA-I stimulated	--
11	chr14:25101800-25103400	Active TSS	Primary T killer naive cells fromperipheralblood	blood

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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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