Variant report

Variant	rs6104756
Chromosome Location	chr20:11453765-11453766
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11698237	1.00[AMR][1000 genomes]
rs13433255	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2207115	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57336143	1.00[AMR][1000 genomes]
rs58524115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58755628	1.00[AMR][1000 genomes]
rs60417076	0.95[AFR][1000 genomes]
rs60852377	1.00[AMR][1000 genomes]
rs6104758	1.00[AFR][1000 genomes]
rs6104762	0.95[AFR][1000 genomes]
rs6108971	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6108972	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6108973	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6108984	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6108987	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6108991	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6109007	1.00[AFR][1000 genomes]
rs6109008	0.95[AFR][1000 genomes]
rs6109016	0.95[AFR][1000 genomes]
rs6109017	0.95[AFR][1000 genomes]
rs6109018	0.95[AFR][1000 genomes]
rs6109019	0.95[AFR][1000 genomes]
rs61136676	1.00[AMR][1000 genomes]
rs7267502	1.00[AMR][1000 genomes]
rs73896349	1.00[AMR][1000 genomes]
rs73896362	1.00[AMR][1000 genomes]
rs73896367	1.00[AMR][1000 genomes]
rs73896368	1.00[AMR][1000 genomes]
rs73896370	1.00[AMR][1000 genomes]
rs73896387	1.00[AMR][1000 genomes]
rs73896399	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73896400	1.00[AMR][1000 genomes]
rs73899009	1.00[AMR][1000 genomes]
rs977277	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065969	chr20:10850562-11464172	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv544181	chr20:10850562-11464172	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv432099	chr20:11371093-11476900	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1058734	chr20:11389232-11479953	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv522929	chr20:11411026-11516418	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:11440200-11454400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:11449000-11457800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr20:11451600-11453800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr20:11452000-11454000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr20:11453400-11455600	Enhancers	Foreskin Melanocyte Primary Cells skin03	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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