Variant report

Variant	rs72984855
Chromosome Location	chr1:75810567-75810568
allele	A/G
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:8)

rs_ID	r²[population]
rs1249832	1.00[EUR][1000 genomes]
rs1249833	1.00[EUR][1000 genomes]
rs1249834	1.00[EUR][1000 genomes]
rs1249835	1.00[EUR][1000 genomes]
rs17096287	1.00[EUR][1000 genomes]
rs4436341	1.00[EUR][1000 genomes]
rs6670185	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72984870	1.00[AMR][1000 genomes];1.00[EUR][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	esv3368999	chr1:75524762-75933220	Bivalent/Poised TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1013952	chr1:75716654-75936048	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv535004	chr1:75716654-75936048	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75807000-75812400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:75808400-75811200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr1:75808800-75811600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr1:75808800-75813000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:75809000-75811000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:75809000-75811200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:75809800-75811000	Enhancers	NH-A	brain
8	chr1:75809800-75811200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:75810400-75811400	Enhancers	HUVEC	blood vessel
10	chr1:75810400-75811800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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