Variant report

Variant	rs7739832
Chromosome Location	chr6:37615199-37615200
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs62398385	1.00[ASN][1000 genomes]
rs62398392	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62398393	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6924003	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs804832	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs804833	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs804857	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs804858	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[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	esv2752124	chr6:37416219-37680622	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv1024016	chr6:37567651-37981590	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37594000-37615400	Weak transcription	Fetal Brain Female	brain
2	chr6:37599200-37615600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:37599200-37621800	Weak transcription	NHLF	lung
4	chr6:37602200-37616600	Weak transcription	Right Atrium	heart
5	chr6:37602800-37616400	Weak transcription	Ovary	ovary
6	chr6:37606800-37615600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:37611800-37616000	Weak transcription	Gastric	stomach
8	chr6:37612200-37615600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:37612200-37616200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr6:37612200-37616200	Weak transcription	GM12878-XiMat	blood
11	chr6:37612400-37615400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:37612400-37616200	Weak transcription	HMEC	breast
13	chr6:37612600-37616000	Weak transcription	Primary B cells from peripheral blood	blood
14	chr6:37612600-37616200	Weak transcription	Left Ventricle	heart
15	chr6:37612600-37619800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr6:37612800-37616000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr6:37613400-37616000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr6:37614200-37615800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:37614200-37621800	Weak transcription	Aorta	Aorta

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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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