Variant report

Variant	rs577612958
Chromosome Location	chr20:22655678-22655679
allele	-/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3520132	chr20:22654499-22657229	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
2	esv3454212	chr20:22655204-22655751	Weak transcription	n/a	n/a	inside rSNPs	n/a
3	esv3520136	chr20:22655234-22655764	Weak transcription	n/a	n/a	inside rSNPs	n/a
4	esv3520135	chr20:22655245-22655707	Weak transcription	n/a	n/a	inside rSNPs	n/a
5	esv3520137	chr20:22655246-22655771	Weak transcription	n/a	n/a	inside rSNPs	n/a
6	esv3520133	chr20:22655253-22655742	Weak transcription	n/a	n/a	inside rSNPs	n/a
7	esv3454210	chr20:22655257-22655801	Weak transcription	n/a	n/a	inside rSNPs	n/a
8	esv3454213	chr20:22655260-22655723	Weak transcription	n/a	n/a	inside rSNPs	n/a
9	esv3454211	chr20:22655273-22655679	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22645600-22664400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:22652200-22659200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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