Variant report

Variant	rs1335926
Chromosome Location	chr1:221099098-221099099
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1335925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56293922	1.00[AMR][1000 genomes]
rs59851594	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60446380	1.00[AMR][1000 genomes]
rs73097489	1.00[AMR][1000 genomes]
rs73107111	1.00[AMR][1000 genomes]
rs74140841	1.00[AMR][1000 genomes]
rs74140843	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74140844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74141254	1.00[AMR][1000 genomes]
rs74141255	1.00[AMR][1000 genomes]
rs74141256	1.00[AMR][1000 genomes]
rs74141257	1.00[AMR][1000 genomes]
rs74141293	1.00[AMR][1000 genomes]
rs7550673	1.00[AMR][1000 genomes]
rs945446	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	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221094400-221099200	Weak transcription	Psoas Muscle	Psoas
2	chr1:221095600-221100800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:221096600-221099200	Weak transcription	Fetal Muscle Leg	muscle
4	chr1:221096600-221099600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr1:221096600-221100200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:221096600-221100800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:221096600-221100800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:221096800-221099200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:221097000-221099400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:221098000-221100600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:221098000-221100600	Enhancers	NHDF-Ad	bronchial
12	chr1:221098200-221099200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:221098200-221100400	Enhancers	Osteobl	bone
14	chr1:221098600-221100400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:221099000-221099600	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr1:221099000-221100200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:221099000-221100400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:221099000-221100600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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

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