Variant report

Variant	rs60847735
Chromosome Location	chr9:100510853-100510854
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1512262	0.94[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1512263	0.80[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs16924016	0.80[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs16924040	0.82[EUR][1000 genomes]
rs16924042	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs16924053	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs57489136	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59320519	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60789150	0.85[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs73484450	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73484452	0.80[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs73484459	0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs73484460	0.95[EUR][1000 genomes]
rs73484463	0.95[EUR][1000 genomes]
rs73484465	0.81[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs73484466	0.95[EUR][1000 genomes]
rs73484469	0.95[EUR][1000 genomes]
rs73484472	0.82[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	nsv1043753	chr9:100458109-100599265	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv614934	chr9:100482976-100550253	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100504000-100514000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:100507200-100513600	Enhancers	Fetal Intestine Small	intestine
3	chr9:100509000-100511000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr9:100509000-100513200	Enhancers	Fetal Intestine Large	intestine
5	chr9:100509200-100511000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:100509400-100511200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:100509400-100511400	Enhancers	HSMMtube	muscle
8	chr9:100509400-100511600	Enhancers	Adipose Nuclei	Adipose
9	chr9:100509600-100511000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:100509600-100511000	Enhancers	Esophagus	oesophagus
11	chr9:100509600-100511200	Enhancers	Placenta	Placenta
12	chr9:100510600-100511400	Bivalent Enhancer	HSMM	muscle
13	chr9:100510800-100511000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr9:100510800-100511000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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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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