Variant report

Variant	rs7036874
Chromosome Location	chr9:110640158-110640159
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10115778	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10816583	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10979080	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10979081	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10979086	0.80[EUR][1000 genomes]
rs12552179	0.85[ASN][1000 genomes]
rs13298965	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4509400	0.81[EUR][1000 genomes]
rs7021395	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7035211	0.84[EUR][1000 genomes]
rs7037236	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7045461	1.00[CHB][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs944472	0.80[CEU][hapmap];0.84[EUR][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	nsv1051101	chr9:110548257-110697253	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110635800-110656800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:110638600-110642200	Weak transcription	Fetal Muscle Leg	muscle
3	chr9:110638800-110640200	Weak transcription	Primary B cells from cord blood	blood
4	chr9:110638800-110640600	Weak transcription	Primary B cells from peripheral blood	blood
5	chr9:110638800-110642200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:110638800-110642400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr9:110639000-110642200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:110639000-110642200	Weak transcription	Osteobl	bone
9	chr9:110639200-110640200	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr9:110640000-110641800	Enhancers	Monocytes-CD14+_RO01746	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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