Variant report

Variant	rs191516372
Chromosome Location	chr4:76479983-76479984
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594687	chr4:76154064-76502748	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv534570	chr4:76214619-76498362	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	esv2525937	chr4:76479338-76480842	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
4	esv1982084	chr4:76479496-76480187	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3520317	chr4:76479572-76480067	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3467203	chr4:76479592-76480062	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3467202	chr4:76479660-76479988	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3520316	chr4:76479670-76479986	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3467204	chr4:76479674-76479984	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3520318	chr4:76479674-76479984	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76458400-76480800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr4:76458800-76480600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr4:76458800-76480600	Weak transcription	Duodenum Mucosa	Duodenum
4	chr4:76465800-76480600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr4:76468400-76480800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:76469200-76480200	Weak transcription	NHEK	skin
7	chr4:76470600-76480600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:76471200-76480400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:76471800-76480800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:76472400-76480400	Weak transcription	HMEC	breast
11	chr4:76473200-76480400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:76473600-76480600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr4:76474800-76480800	Weak transcription	HSMMtube	muscle
14	chr4:76475000-76480200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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