Variant report

Variant	rs142747463
Chromosome Location	chr4:153143552-153143553
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv931416	chr4:152877808-153440553	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv964324	chr4:153143531-153149109	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:153141600-153143600	Enhancers	Primary T cells fromperipheralblood	blood
2	chr4:153141600-153143600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr4:153142000-153143600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr4:153142000-153145400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:153142600-153143600	Enhancers	Primary T cells from cord blood	blood
6	chr4:153142800-153143600	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr4:153143000-153143600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr4:153143000-153143600	Enhancers	Dnd41	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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