Variant report

Variant	rs553268026
Chromosome Location	chr6:133785801-133785802
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3435687	chr6:133785679-133785891	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133765800-133822000	Weak transcription	Psoas Muscle	Psoas
2	chr6:133778400-133789000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr6:133780800-133796800	Weak transcription	NHLF	lung
4	chr6:133782000-133789600	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:133782000-133790400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr6:133782000-133811600	Weak transcription	A549	lung
7	chr6:133782200-133790000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:133782400-133806400	Weak transcription	Fetal Muscle Leg	muscle
9	chr6:133784000-133813000	Weak transcription	HSMMtube	muscle
10	chr6:133784200-133789400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr6:133785800-133786600	Weak transcription	Hela-S3	cervix
12	chr6:133785800-133787800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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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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