Variant report

Variant	rs531750876
Chromosome Location	chr21:17378096-17378097
allele	C/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	nsv1064664	chr21:17336936-17405756	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3424252	chr21:17377892-17378940	Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv3455307	chr21:17377907-17378974	Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv3455309	chr21:17377907-17378974	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3507945	chr21:17378063-17378957	Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3507946	chr21:17378066-17378921	Weak transcription	n/a	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	chr21:17376600-17380400	Weak transcription	Osteobl	bone

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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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