Variant report

Variant	rs73591395
Chromosome Location	chr6:128923763-128923764
allele	C/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:16)

rs_ID	r²[population]
rs1341586	1.00[EUR][1000 genomes]
rs17055961	1.00[EUR][1000 genomes]
rs17055964	1.00[EUR][1000 genomes]
rs17055978	1.00[EUR][1000 genomes]
rs17055990	1.00[EUR][1000 genomes]
rs17056023	1.00[EUR][1000 genomes]
rs17056041	1.00[EUR][1000 genomes]
rs17056045	1.00[EUR][1000 genomes]
rs17056084	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17056088	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59615501	1.00[EUR][1000 genomes]
rs6569534	1.00[EUR][1000 genomes]
rs6921512	0.83[AMR][1000 genomes]
rs73591394	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73772055	1.00[EUR][1000 genomes]
rs73772058	1.00[EUR][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	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv830801	chr6:128878436-129064667	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128920000-128928800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:128922200-128924000	Weak transcription	Left Ventricle	heart
3	chr6:128922200-128927000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:128922400-128927000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:128922600-128926800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:128922600-128927200	Weak transcription	NHDF-Ad	bronchial
7	chr6:128922800-128926400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr6:128922800-128926800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr6:128922800-128927000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:128922800-128927000	Weak transcription	Osteobl	bone
11	chr6:128923200-128926400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr6:128923200-128927000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:128923400-128923800	Enhancers	HUVEC	blood vessel
14	chr6:128923400-128925800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:128923400-128925800	Weak transcription	NHEK	skin
16	chr6:128923400-128926800	Weak transcription	HMEC	breast
17	chr6:128923600-128924200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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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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