Variant report

Variant	rs7219279
Chromosome Location	chr17:66622237-66622238
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12150134	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2159332	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2907392	0.84[EUR][1000 genomes]
rs2907393	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2952310	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4968905	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4968906	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs58171668	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9915019	0.88[AMR][1000 genomes];0.81[EUR][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	nsv833524	chr17:66524030-66705194	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv908693	chr17:66619054-66647840	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66610000-66624200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr17:66618800-66624200	Weak transcription	Osteobl	bone
3	chr17:66619400-66624000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr17:66620600-66622400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr17:66621200-66624000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr17:66621200-66624000	Weak transcription	Placenta	Placenta
7	chr17:66621200-66624000	Weak transcription	Ovary	ovary
8	chr17:66621200-66624000	Weak transcription	HMEC	breast
9	chr17:66621800-66624200	Weak transcription	Esophagus	oesophagus

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