Variant report

Variant	rs73617882
Chromosome Location	chr13:110364978-110364979
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2099434	1.00[AMR][1000 genomes]
rs57251560	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57484686	1.00[AMR][1000 genomes]
rs73617861	1.00[AMR][1000 genomes]
rs73617873	1.00[AMR][1000 genomes]
rs7989944	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044855	chr13:110301572-110408608	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110359000-110367800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr13:110359800-110368400	Weak transcription	Hela-S3	cervix
3	chr13:110360000-110367800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:110360600-110368000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr13:110361000-110368200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr13:110361000-110368200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr13:110363600-110367600	Weak transcription	Liver	Liver
8	chr13:110364200-110365000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr13:110364400-110365000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr13:110364400-110365000	Enhancers	Fetal Intestine Small	intestine
11	chr13:110364400-110365000	Enhancers	Fetal Kidney	kidney
12	chr13:110364600-110365000	Enhancers	Fetal Lung	lung
13	chr13:110364600-110365000	Enhancers	K562	blood
14	chr13:110364600-110365200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr13:110364800-110365000	Weak transcription	Stomach Mucosa	stomach
16	chr13:110364800-110365000	Enhancers	Dnd41	blood
17	chr13:110364800-110368400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr13:110364800-110368400	Weak transcription	HUES64 Cell Line	embryonic stem cell

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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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