Variant report

Variant	rs300955
Chromosome Location	chr4:144203121-144203122
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000250969	TF binding region
ENSG00000250326	Chromatin interaction
ENSG00000170185	Chromatin interaction
ENSG00000178972	Chromatin interaction
ENSG00000109458	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11941277	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11941986	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11942185	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13105156	1.00[CHB][hapmap]
rs13133540	1.00[CHB][hapmap]
rs13146448	1.00[CHB][hapmap]
rs182467	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs188521	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs214426	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28397211	1.00[ASN][1000 genomes]
rs300948	0.90[EUR][1000 genomes]
rs300950	1.00[CHB][hapmap]
rs300954	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34420992	1.00[ASN][1000 genomes]
rs522027	1.00[ASN][1000 genomes]
rs535824	1.00[ASN][1000 genomes]
rs536660	1.00[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	nsv1033902	chr4:144114413-144285772	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv880177	chr4:144174773-144214082	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:144202000-144203800	Enhancers	Fetal Lung	lung
2	chr4:144202000-144203800	Enhancers	Fetal Stomach	stomach
3	chr4:144202400-144203800	Enhancers	Fetal Muscle Leg	muscle
4	chr4:144202600-144203800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:144202600-144204200	Enhancers	Fetal Muscle Trunk	muscle
6	chr4:144202800-144203200	Enhancers	GM12878-XiMat	blood
7	chr4:144202800-144204000	Enhancers	Adipose Nuclei	Adipose
8	chr4:144203000-144203200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:144203000-144203400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:144203000-144203400	Enhancers	Fetal Brain Male	brain
11	chr4:144203000-144203600	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr4:144203000-144203800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:144203000-144203800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:144203000-144204600	Enhancers	NHDF-Ad	bronchial

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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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