Variant report

Variant	rs73784844
Chromosome Location	chr6:164210071-164210072
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs59096961	1.00[AMR][1000 genomes]
rs59173227	0.90[AFR][1000 genomes]
rs60334591	0.90[AFR][1000 genomes]
rs6920091	0.90[AFR][1000 genomes]
rs73784840	0.84[AFR][1000 genomes]
rs73784842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73784855	0.90[AFR][1000 genomes]
rs73784862	0.85[AFR][1000 genomes];1.00[AMR][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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164204000-164210400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:164204000-164210600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:164204400-164210200	Weak transcription	GM12878-XiMat	blood
4	chr6:164208200-164210600	Enhancers	K562	blood
5	chr6:164208400-164211400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:164209200-164210800	Enhancers	Psoas Muscle	Psoas
7	chr6:164209200-164211600	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr6:164209200-164212000	Enhancers	Fetal Muscle Leg	muscle
9	chr6:164209400-164211600	Enhancers	Skeletal Muscle Female	skeletal muscle

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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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