Variant report

Variant	rs7872217
Chromosome Location	chr9:21573443-21573444
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10118880	0.86[ASN][1000 genomes]
rs10124312	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10126000	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1013241	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7033598	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9298817	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031432	chr9:21472601-21608774	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases
2	nsv540085	chr9:21472601-21608774	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases
3	nsv1029634	chr9:21542970-21765286	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21565600-21576000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr9:21568200-21576200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr9:21571000-21574200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:21571000-21575600	Weak transcription	NHDF-Ad	bronchial
5	chr9:21571200-21575600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr9:21571200-21575600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr9:21571200-21575600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr9:21571200-21575600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:21571200-21575800	Weak transcription	NHLF	lung
10	chr9:21571800-21574200	Weak transcription	NH-A	brain
11	chr9:21571800-21575600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr9:21572200-21573800	Enhancers	A549	lung
13	chr9:21572200-21574000	Weak transcription	Hela-S3	cervix
14	chr9:21572200-21575400	Weak transcription	HMEC	breast
15	chr9:21572800-21575400	Weak transcription	NHEK	skin
16	chr9:21573200-21575000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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