Variant report

Variant	rs6763056
Chromosome Location	chr3:69773796-69773797
allele	C/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	chr3:69770114..69772168-chr3:69772406..69774222,2	K562	blood:
2	chr3:69773057..69775025-chr3:69780234..69782973,2	K562	blood:
3	chr3:69773033..69775025-chr3:69780234..69783235,3	K562	blood:
4	chr3:69766513..69768350-chr3:69772258..69773911,2	K562	blood:
5	chr3:69766513..69769005-chr3:69772258..69773911,3	K562	blood:
6	chr3:69771834..69774322-chr3:69822965..69825784,2	K562	blood:
7	chr3:69772543..69775143-chr3:69789277..69791616,2	K562	blood:
8	chr3:69773279..69775300-chr3:69812499..69814226,2	K562	blood:

No data

No data

No data

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3426797	chr3:69433086-69777229	Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv834723	chr3:69643641-69811601	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69761800-69778400	Weak transcription	Right Atrium	heart
2	chr3:69768400-69773800	Weak transcription	Left Ventricle	heart
3	chr3:69768600-69774000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:69769800-69774000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:69769800-69775400	Weak transcription	Psoas Muscle	Psoas
6	chr3:69770200-69773800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr3:69771200-69774000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr3:69772200-69775800	Enhancers	Fetal Heart	heart
9	chr3:69772800-69773800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:69772800-69773800	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr3:69772800-69774200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr3:69773600-69775400	Flanking Active TSS	K562	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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