Variant report

Variant	rs6137760
Chromosome Location	chr20:22795200-22795201
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs6036224	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6048357	0.99[EUR][1000 genomes]
rs6048360	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6082845	0.97[EUR][1000 genomes]
rs6082847	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6082861	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6082863	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6082864	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6132548	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6137759	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6137761	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62201996	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv912816	chr20:22757960-23062927	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv3334	chr20:22773462-22818362	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 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	chr20:22786400-22796600	Weak transcription	HSMMtube	muscle
2	chr20:22790200-22795600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:22792000-22795200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr20:22792400-22795600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:22792400-22795600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr20:22792400-22799000	Weak transcription	Placenta	Placenta
7	chr20:22792600-22796400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr20:22793800-22796800	Enhancers	Dnd41	blood
9	chr20:22794400-22795200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr20:22794400-22797200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr20:22794600-22796200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr20:22794600-22797200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr20:22794800-22795400	Enhancers	Stomach Mucosa	stomach
14	chr20:22794800-22795600	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr20:22794800-22797000	Enhancers	Primary hematopoietic stem cells	blood
16	chr20:22795000-22797200	Enhancers	Fetal Muscle Leg	muscle
17	chr20:22795200-22795600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links