Variant report

Variant	rs10919434
Chromosome Location	chr1:170548180-170548181
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10733056	1.00[AMR][1000 genomes]
rs10753814	1.00[AMR][1000 genomes]
rs10753815	1.00[AMR][1000 genomes]
rs10919425	1.00[AMR][1000 genomes]
rs12062348	1.00[AMR][1000 genomes]
rs12072089	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12087798	1.00[AMR][1000 genomes]
rs12088253	1.00[AMR][1000 genomes]
rs12116909	1.00[AMR][1000 genomes]
rs1333133	1.00[AMR][1000 genomes]
rs1333156	1.00[AMR][1000 genomes]
rs1412895	1.00[AMR][1000 genomes]
rs1537397	1.00[AMR][1000 genomes]
rs1576980	1.00[AMR][1000 genomes]
rs1855221	1.00[AMR][1000 genomes]
rs2104918	1.00[AMR][1000 genomes]
rs2150029	1.00[AMR][1000 genomes]
rs2225322	1.00[AMR][1000 genomes]
rs2901401	1.00[AMR][1000 genomes]
rs4233350	1.00[AMR][1000 genomes]
rs4656769	1.00[AMR][1000 genomes]
rs4656775	1.00[AMR][1000 genomes]
rs4656777	1.00[AMR][1000 genomes]
rs4656779	1.00[AMR][1000 genomes]
rs57462154	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57674813	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6657164	1.00[AMR][1000 genomes]
rs6660575	1.00[AMR][1000 genomes]
rs6676081	1.00[AMR][1000 genomes]
rs6680083	1.00[AMR][1000 genomes]
rs6703801	1.00[AMR][1000 genomes]
rs7531125	1.00[AMR][1000 genomes]
rs7538125	1.00[AMR][1000 genomes]
rs7548443	1.00[AMR][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	nsv872543	chr1:170171083-170674903	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv533915	chr1:170258766-170725296	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170537800-170549800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr1:170547200-170549200	Enhancers	NHDF-Ad	bronchial
3	chr1:170547200-170551200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:170547400-170548200	Enhancers	Osteobl	bone
5	chr1:170547800-170548200	Enhancers	Dnd41	blood
6	chr1:170548000-170548200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:170548000-170548400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:170548000-170549000	Enhancers	Foreskin Fibroblast Primary Cells skin01	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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