Variant report

Variant	rs2806970
Chromosome Location	chr13:53650158-53650159
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs2491126	0.83[AFR][1000 genomes]
rs2759673	0.83[AFR][1000 genomes]
rs2759683	0.83[AFR][1000 genomes]
rs2759684	0.83[AFR][1000 genomes]
rs2759686	0.83[AFR][1000 genomes]
rs2759687	0.83[AFR][1000 genomes]
rs2759689	0.83[AFR][1000 genomes]
rs2759692	0.87[AFR][1000 genomes]
rs2799342	0.88[AFR][1000 genomes]
rs2806993	0.87[AFR][1000 genomes]
rs2807005	0.83[AFR][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	nsv530719	chr13:53173014-53675953	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv3440613	chr13:53307609-53671072	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv832613	chr13:53524319-53687188	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53639200-53654800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr13:53647200-53651600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr13:53647400-53650800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:53647400-53651600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr13:53648200-53650400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr13:53648800-53651200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr13:53649200-53650400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr13:53649400-53651000	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr13:53649600-53650200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:53649600-53650200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr13:53649600-53651600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr13:53649800-53650200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr13:53650000-53652400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:53650000-53653400	Weak transcription	H1 BMP4 Derived Trophoblast 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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