Variant report

Variant	rs34844672
Chromosome Location	chr9:110702934-110702935
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10512375	0.84[EUR][1000 genomes]
rs10512376	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10816591	0.89[AFR][1000 genomes]
rs10816592	0.80[AFR][1000 genomes]
rs10816593	0.80[AFR][1000 genomes]
rs10979114	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10979119	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12340808	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12343242	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12351443	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1339761	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34116013	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35960909	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59994319	0.88[EUR][1000 genomes]
rs6477606	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7041168	0.91[AFR][1000 genomes]
rs7867441	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[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	nsv893701	chr9:110650482-110709587	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110695800-110705200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr9:110696200-110707800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:110701200-110703800	Enhancers	Placenta Amnion	Placenta Amnion
4	chr9:110701600-110705000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr9:110702200-110711000	Weak transcription	Fetal Intestine Large	intestine
6	chr9:110702400-110703800	Enhancers	Fetal Stomach	stomach
7	chr9:110702600-110704200	Weak transcription	Spleen	Spleen
8	chr9:110702800-110703400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr9:110702800-110703800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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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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