Variant report

Variant	rs528004136
Chromosome Location	chr1:71247039-71247040
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3452325	chr1:71243992-71249701	Active TSS Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
2	esv3452326	chr1:71244085-71249601	Flanking Active TSS Enhancers Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
3	esv3452327	chr1:71244085-71249601	Enhancers Weak transcription Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
4	esv18463	chr1:71244106-71249573	Enhancers Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
5	nsv546459	chr1:71245142-71247531	Flanking Active TSS Enhancers Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
6	nsv546460	chr1:71245142-71248283	Flanking Active TSS Enhancers Active TSS Weak transcription	lncRNA	n/a	inside rSNPs	diseases
7	nsv546461	chr1:71245142-71249139	Enhancers Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
8	nsv546462	chr1:71245142-71249485	Enhancers Weak transcription Active TSS Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
9	nsv546464	chr1:71245423-71247822	Enhancers Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
10	nsv546465	chr1:71245423-71249139	Enhancers Weak transcription Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
11	nsv546466	chr1:71245423-71249485	Flanking Active TSS Enhancers Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
12	nsv546467	chr1:71245703-71249485	Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	inside rSNPs	diseases
13	nsv546468	chr1:71246040-71247531	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
14	nsv546469	chr1:71246040-71249139	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
15	nsv546470	chr1:71246443-71248198	Enhancers	lncRNA	n/a	inside rSNPs	diseases

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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