Variant report

Variant	rs528697944
Chromosome Location	chr6:73362730-73362731
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023809	chr6:73157813-73477997	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538303	chr6:73157813-73477997	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3347486	chr6:73283590-73445976	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3472802	chr6:73361866-73365223	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3472803	chr6:73361891-73365203	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3472804	chr6:73361891-73365203	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv823730	chr6:73361941-73365099	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73336200-73362800	Weak transcription	Primary B cells from cord blood	blood
2	chr6:73359600-73362800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr6:73359600-73373000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:73359600-73398800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr6:73359800-73386800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr6:73360400-73372600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:73361000-73367200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:73361800-73362800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:73361800-73367200	Weak transcription	NHEK	skin
10	chr6:73362000-73363200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:73362200-73362800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr6:73362200-73362800	Enhancers	Fetal Heart	heart
13	chr6:73362400-73367200	Weak transcription	Osteobl	bone
14	chr6:73362600-73363200	Flanking Active TSS	GM12878-XiMat	blood
15	chr6:73362600-73365200	Weak transcription	Aorta	Aorta
16	chr6:73362600-73367200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr6:73362600-73371600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:73362600-73379200	Weak transcription	Psoas Muscle	Psoas

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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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