Variant report

Variant	rs6887284
Chromosome Location	chr5:152022828-152022829
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10043260	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10515674	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12655993	0.93[ASN][1000 genomes]
rs12658941	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17456094	0.80[ASN][1000 genomes]
rs17564660	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2961750	0.90[ASN][1000 genomes]
rs2964258	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6579952	0.90[ASN][1000 genomes]
rs6873744	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797295	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7720912	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023676	chr5:151979253-152925064	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv537927	chr5:151979253-152925064	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv5074	chr5:152010691-152055779	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:152015000-152024000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr5:152021000-152024200	Enhancers	Fetal Brain Male	brain
3	chr5:152021400-152023000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
4	chr5:152021400-152023000	Enhancers	Placenta Amnion	Placenta Amnion
5	chr5:152021600-152023200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr5:152021800-152023800	Weak transcription	Fetal Brain Female	brain
7	chr5:152022000-152024400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
8	chr5:152022200-152023000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr5:152022200-152024400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
10	chr5:152022200-152029400	Weak transcription	Aorta	Aorta
11	chr5:152022400-152023000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:152022400-152023000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:152022400-152023800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:152022400-152024600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:152022600-152023000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr5:152022600-152023400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr5:152022600-152024400	Enhancers	Fetal Kidney	kidney
18	chr5:152022800-152023000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:152022800-152023800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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