Variant report

Variant	rs645194
Chromosome Location	chr1:46903915-46903916
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs4660934	0.91[EUR][1000 genomes]
rs547581	0.92[EUR][1000 genomes]
rs618127	0.95[EUR][1000 genomes]
rs661902	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7513864	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005189	chr1:46335186-46949309	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv534946	chr1:46335186-46949309	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	esv2761743	chr1:46339858-47026743	Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv1000562	chr1:46832451-47027044	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr1:46872800-46908000	Weak transcription	Right Atrium	heart
2	chr1:46882000-46908200	Weak transcription	Brain Anterior Caudate	brain
3	chr1:46890800-46908200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:46899800-46908200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr1:46901800-46907800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:46902200-46904600	Enhancers	K562	blood
7	chr1:46902200-46908000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:46902600-46908200	Weak transcription	Esophagus	oesophagus
9	chr1:46903000-46904000	Enhancers	Gastric	stomach
10	chr1:46903000-46904600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:46903400-46904400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr1:46903400-46904600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:46903600-46904000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:46903600-46904200	Enhancers	GM12878-XiMat	blood
15	chr1:46903800-46904000	Enhancers	Primary hematopoietic stem cells	blood
16	chr1:46903800-46904000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:46903800-46908000	Weak transcription	Primary monocytes fromperipheralblood	blood

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