Variant report

Variant	rs7642393
Chromosome Location	chr3:112540576-112540577
allele	A/G
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:15)

rs_ID	r²[population]
rs1125377	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11918522	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1500877	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16860127	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1948164	0.83[ASN][1000 genomes]
rs2078008	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4682117	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs66635385	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6809029	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72950327	0.81[ASN][1000 genomes]
rs7610094	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7625445	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7625533	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7628337	0.81[ASN][1000 genomes]
rs7642984	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv432477	chr3:112390310-112603310	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv877343	chr3:112470586-112597706	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr3:112533200-112543200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:112537200-112541000	Weak transcription	NHLF	lung
3	chr3:112537800-112543200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr3:112538600-112541000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr3:112539800-112540800	Enhancers	Primary B cells from cord blood	blood
6	chr3:112540000-112541200	Enhancers	Primary B cells from peripheral blood	blood
7	chr3:112540000-112542400	Flanking Active TSS	A549	lung
8	chr3:112540200-112541600	Weak transcription	Fetal Kidney	kidney
9	chr3:112540400-112541000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr3:112540400-112542200	Enhancers	Hela-S3	cervix

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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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