Variant report

Variant	rs575372552
Chromosome Location	chr14:81589407-81589408
allele	G/T
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	nsv1052999	chr14:81468860-81599074	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv542144	chr14:81468860-81599074	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv832841	chr14:81588322-81743921	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	86 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81538200-81593000	Weak transcription	Psoas Muscle	Psoas
2	chr14:81572600-81591400	Weak transcription	Liver	Liver
3	chr14:81579800-81591800	Weak transcription	Thymus	Thymus
4	chr14:81579800-81591800	Weak transcription	Dnd41	blood
5	chr14:81581000-81593200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr14:81586400-81589800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr14:81586800-81592200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr14:81587800-81589800	Weak transcription	Primary B cells from cord blood	blood
9	chr14:81588600-81589600	Enhancers	GM12878-XiMat	blood
10	chr14:81589200-81589800	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr14:81589400-81592000	Weak transcription	Primary B cells from peripheral 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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