Variant report

Variant	rs28691054
Chromosome Location	chr7:138419412-138419413
allele	A/G
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:9)

rs_ID	r²[population]
rs13246226	1.00[EUR][1000 genomes]
rs13246294	1.00[EUR][1000 genomes]
rs3807149	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3807152	1.00[EUR][1000 genomes]
rs56317995	1.00[EUR][1000 genomes]
rs56983691	1.00[EUR][1000 genomes]
rs6972218	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73730479	1.00[EUR][1000 genomes]
rs73730493	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030956	chr7:138163169-138579519	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138400600-138439000	Weak transcription	Right Atrium	heart
2	chr7:138403400-138420200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:138414800-138425800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:138419200-138419600	Weak transcription	H9 Cell Line	embryonic stem cell

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