Variant report

Variant	rs571890985
Chromosome Location	chr4:144042678-144042679
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034895	chr4:143945139-144079655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2450073	chr4:144041359-144043213	Inactive region	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
3	esv3467404	chr4:144042263-144042923	Inactive region	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
4	esv3467405	chr4:144042336-144042850	Inactive region	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
5	esv2561273	chr4:144042349-144042844	Inactive region	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
6	esv3467406	chr4:144042350-144042849	Inactive region	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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