Variant report

Variant	rs3212245
Chromosome Location	chr14:24809957-24809958
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000129467	Chromatin interaction
ENSG00000157379	Chromatin interaction
ENSG00000100441	Chromatin interaction
ENSG00000139899	Chromatin interaction
ENSG00000196943	Chromatin interaction
ENSG00000100445	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10483285	0.90[CHB][hapmap];0.84[ASN][1000 genomes]
rs1124644	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs12895908	0.98[ASN][1000 genomes]
rs17102976	0.89[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2332324	0.97[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs28561820	0.86[ASN][1000 genomes]
rs3212241	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3212254	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs4982897	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57167043	0.86[ASN][1000 genomes]
rs67627083	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24809400-24810000	Enhancers	Primary B cells from peripheral blood	blood
2	chr14:24809400-24813000	Weak transcription	Liver	Liver
3	chr14:24809400-24816200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr14:24809600-24810600	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr14:24809600-24812400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:24809600-24821000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr14:24809800-24810000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr14:24809800-24810600	Weak transcription	Primary B cells from cord blood	blood
9	chr14:24809800-24812600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr14:24809800-24812600	Weak transcription	Fetal Intestine Large	intestine

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

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