Variant report

Variant	rs13375786
Chromosome Location	chr1:45038178-45038179
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:45037140..45040002-chr1:45040486..45044192,4	K562	blood:
2	chr1:45037397..45038432-chr1:45117995..45118774,4	K562	blood:
3	chr1:45037445..45038410-chr1:45060557..45061427,3	K562	blood:
4	chr1:45036529..45039222-chr1:45046512..45048986,2	K562	blood:
5	chr1:45038059..45040987-chr1:45041821..45044367,3	K562	blood:
6	chr1:45035189..45038471-chr1:45096120..45099117,3	K562	blood:
7	chr1:45037501..45038399-chr1:45060218..45061438,4	MCF-7	breast:
8	chr1:45036529..45039444-chr1:45046512..45048459,3	K562	blood:

No data

No data

No data

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12069382	1.00[AMR][1000 genomes]
rs13373830	0.96[AFR][1000 genomes]
rs35789261	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533037	chr1:44361728-45333408	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
2	nsv1004861	chr1:44843654-45210176	Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	346 gene(s)	inside rSNPs	diseases
3	nsv534940	chr1:44843654-45210176	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	346 gene(s)	inside rSNPs	diseases
4	nsv461395	chr1:44898998-45119965	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
5	nsv546144	chr1:44898998-45119965	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
6	nsv998476	chr1:45001278-45311757	Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
7	nsv534941	chr1:45001278-45311757	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45018000-45082600	Weak transcription	Right Atrium	heart
2	chr1:45023800-45047600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:45029400-45038400	Enhancers	Brain Cingulate Gyrus	brain
4	chr1:45029800-45047800	Enhancers	Brain Hippocampus Middle	brain
5	chr1:45031200-45040000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr1:45032200-45041000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr1:45032400-45042000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:45033400-45039800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:45034400-45039800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:45035400-45039800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:45036200-45039000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:45036800-45044200	Enhancers	Brain Substantia Nigra	brain
13	chr1:45037000-45038600	Enhancers	Brain Angular Gyrus	brain
14	chr1:45037600-45038600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr1:45037600-45039200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr1:45037600-45040200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr1:45037800-45038200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:45038000-45038400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:45038000-45039400	Weak transcription	Brain Anterior Caudate	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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