Variant report

Variant	rs35665189
Chromosome Location	chr21:28177984-28177985
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs13046223	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13050530	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13051175	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1822623	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2830547	0.90[AMR][1000 genomes]
rs34542237	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35612760	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56213639	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59830135	1.00[AMR][1000 genomes]
rs60964152	1.00[AMR][1000 genomes]
rs66740819	1.00[AMR][1000 genomes]
rs71317486	1.00[AMR][1000 genomes]
rs7277043	1.00[AMR][1000 genomes]
rs7278460	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7279842	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];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	nsv1066573	chr21:28096356-28374354	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1057400	chr21:28104936-28359948	Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 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	chr21:28170800-28181000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr21:28174000-28178800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr21:28174000-28185400	Weak transcription	HSMMtube	muscle
4	chr21:28174400-28178800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr21:28174600-28187800	Weak transcription	Osteobl	bone
6	chr21:28175000-28178200	Enhancers	Ovary	ovary
7	chr21:28176800-28178200	Enhancers	Hela-S3	cervix
8	chr21:28177000-28178200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr21:28177200-28178200	Enhancers	Fetal Stomach	stomach
10	chr21:28177200-28178200	Enhancers	NHDF-Ad	bronchial
11	chr21:28177400-28178000	Enhancers	Stomach Smooth Muscle	stomach
12	chr21:28177400-28178400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr21:28177800-28179400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr21:28177800-28186800	Weak transcription	NHLF	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