Variant report

Variant	rs150934397
Chromosome Location	chr4:105885206-105885207
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:104944123..104945646-chr4:105884836..105887538,2	MCF-7	breast:
2	chr4:105883010..105897017-chr4:106062943..106072055,55	MCF-7	breast:
3	chr4:105829316..105831540-chr4:105884593..105886682,3	MCF-7	breast:
4	chr4:105817342..105819029-chr4:105882567..105885514,2	MCF-7	breast:
5	chr4:105885086..105887081-chr4:105979526..105982369,3	MCF-7	breast:
6	chr4:105877746..105880417-chr4:105883810..105885647,2	MCF-7	breast:
7	chr4:105884036..105898505-chr4:106054854..106072562,138	MCF-7	breast:
8	chr4:105883633..105885382-chr4:105888462..105890781,2	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3341748	chr4:105569622-105903733	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv461609	chr4:105869548-106366209	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv470063	chr4:105869548-106366209	Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv595007	chr4:105869548-106366209	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv830024	chr4:105884350-106037816	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:105884600-105885600	Enhancers	Esophagus	oesophagus
2	chr4:105884800-105886000	ZNF genes & repeats	GM12878-XiMat	blood
3	chr4:105884800-105887600	Weak transcription	Stomach Mucosa	stomach
4	chr4:105885200-105885400	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr4:105885200-105886000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr4:105885200-105887000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:105885200-105887800	Enhancers	Primary neutrophils fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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