Variant report

Variant	rs72762378
Chromosome Location	chr9:118020631-118020632
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1029341	0.84[EUR][1000 genomes]
rs10481680	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10817734	0.82[EUR][1000 genomes]
rs10817741	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10817742	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11998787	0.82[EUR][1000 genomes]
rs12001569	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12338583	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12348813	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2285315	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2418327	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35686252	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4147051	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72762372	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72764238	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7846857	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9987570	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	nsv831697	chr9:117860416-118023927	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv615251	chr9:117975864-118514444	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118014000-118023400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:118014200-118023000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:118014400-118023800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:118015600-118023400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:118016000-118023600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:118017400-118023600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr9:118017600-118023200	Weak transcription	Fetal Muscle Leg	muscle
8	chr9:118018000-118023400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:118018000-118023600	Weak transcription	Colon Smooth Muscle	Colon
10	chr9:118018200-118024000	Weak transcription	Fetal Lung	lung
11	chr9:118018200-118024000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr9:118020200-118023000	Weak transcription	NHEK	skin

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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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