Variant report

Variant	rs73935225
Chromosome Location	chr2:55031093-55031094
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs56063218	0.98[AFR][1000 genomes]
rs59015634	0.84[AFR][1000 genomes]
rs6740845	0.84[AFR][1000 genomes]
rs73935221	0.97[AFR][1000 genomes]
rs73935222	1.00[AFR][1000 genomes]
rs73935223	1.00[AFR][1000 genomes]
rs73935224	0.84[AFR][1000 genomes]
rs73935227	1.00[AFR][1000 genomes]
rs73935663	0.86[AFR][1000 genomes]
rs73935665	0.84[AFR][1000 genomes]
rs73935667	0.81[AFR][1000 genomes]
rs73935669	0.80[AFR][1000 genomes]
rs73935670	0.84[AFR][1000 genomes]
rs73936464	0.82[AFR][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	esv33638	chr2:54765256-55109455	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1005449	chr2:54938633-55129503	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv1844727	chr2:54999712-55084583	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv870295	chr2:55008613-55065985	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv470465	chr2:55010115-55034113	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv874152	chr2:55023600-55060479	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	1 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	chr2:55022200-55031200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr2:55030000-55032000	Enhancers	Brain Germinal Matrix	brain
3	chr2:55030200-55031800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr2:55030200-55031800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr2:55030400-55031600	Enhancers	Fetal Brain Female	brain
6	chr2:55030400-55032000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:55030800-55031400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:55031000-55031400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:55031000-55031600	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr2:55031000-55032000	Enhancers	NHDF-Ad	bronchial

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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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