Variant report

Variant	rs75483527
Chromosome Location	chr12:62393525-62393526
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv559151	chr12:62390768-62394361	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3323443	chr12:62392085-62396383	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv559152	chr12:62392548-62395774	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv1820144	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv1823662	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1843366	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv1844580	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv1848150	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv1850527	chr12:62393257-62394361	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2633161	chr12:62393516-62395086	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62391200-62393600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr12:62392600-62393600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:62392600-62394200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr12:62393200-62393600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:62393400-62396600	Weak transcription	Monocytes-CD14+_RO01746	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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