Variant report

Variant	rs58287896
Chromosome Location	chr2:85694221-85694222
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000118640	Chromatin interaction
ENSG00000168906	Chromatin interaction
ENSG00000266577	Chromatin interaction
ENSG00000115486	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11684647	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34052656	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34619872	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35619560	0.95[ASN][1000 genomes]
rs55846016	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72938532	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005351	chr2:85242657-85774909	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	198 gene(s)	inside rSNPs	diseases
2	nsv535803	chr2:85242657-85774909	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	198 gene(s)	inside rSNPs	diseases
3	nsv834283	chr2:85609500-85755708	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:85684000-85695400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:85684800-85695400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:85685400-85694400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr2:85687000-85695200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:85687000-85695200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:85687000-85695600	Weak transcription	NHDF-Ad	bronchial
7	chr2:85690400-85694400	Weak transcription	Fetal Intestine Large	intestine
8	chr2:85691400-85695200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:85693400-85701400	Enhancers	Fetal Intestine Small	intestine
10	chr2:85693800-85695000	Weak transcription	Colonic Mucosa	Colon
11	chr2:85693800-85695200	Enhancers	A549	lung
12	chr2:85693800-85695800	Enhancers	Hela-S3	cervix
13	chr2:85694000-85695200	Weak transcription	Small Intestine	intestine
14	chr2:85694200-85694600	Enhancers	Stomach Mucosa	stomach
15	chr2:85694200-85695200	Enhancers	HepG2	liver
16	chr2:85694200-85696800	Enhancers	Rectal Mucosa Donor 31	rectum

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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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