Variant report

Variant	rs111288642
Chromosome Location	chr16:81811626-81811627
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv948448	chr16:81198147-81906766	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
2	nsv573365	chr16:81804972-81975892	Strong transcription Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv3372455	chr16:81810851-81815149	Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81792000-81812200	Weak transcription	Right Atrium	heart
2	chr16:81807200-81812200	Weak transcription	Adipose Nuclei	Adipose
3	chr16:81807600-81812400	Weak transcription	Left Ventricle	heart
4	chr16:81808400-81812000	Weak transcription	Fetal Thymus	thymus
5	chr16:81808600-81811800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr16:81808800-81812400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr16:81809600-81811800	Weak transcription	Primary B cells from peripheral blood	blood
8	chr16:81809600-81811800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr16:81809600-81812000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr16:81809600-81812000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr16:81809600-81812200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr16:81809800-81812000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr16:81810200-81812200	Weak transcription	GM12878-XiMat	blood
14	chr16:81810400-81812200	Weak transcription	Placenta	Placenta
15	chr16:81811600-81811800	Bivalent/Poised TSS	K562	blood
16	chr16:81811600-81812200	Enhancers	Primary B cells from cord blood	blood

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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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