Variant report

Variant	rs144433009
Chromosome Location	chr4:175627305-175627306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1018390	chr4:175475505-175969742	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv880584	chr4:175505749-175644689	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3466671	chr4:175623177-175628675	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3359677	chr4:175623727-175628225	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3424636	chr4:175624427-175628125	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3466670	chr4:175624702-175627311	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv1839259	chr4:175625334-175628121	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv1840041	chr4:175625334-175628121	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv1836376	chr4:175625493-175628121	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv596244	chr4:175625493-175631711	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	esv1800533	chr4:175625561-175631986	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	esv1842309	chr4:175625612-175632405	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	esv1839649	chr4:175625688-175628121	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv596257	chr4:175626079-175631711	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
16	nsv596258	chr4:175626104-175631711	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	esv3511868	chr4:175626560-175627937	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3511869	chr4:175626560-175627937	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175624600-175628400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte 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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