Variant report

Variant	rs184417755
Chromosome Location	chr6:54881783-54881784
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3364886	chr6:54880042-54912395	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
2	esv3368520	chr6:54881042-54905736	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54879800-54882400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:54880400-54883200	Enhancers	Fetal Intestine Large	intestine
3	chr6:54880400-54883200	Enhancers	Fetal Lung	lung
4	chr6:54880800-54883400	Enhancers	Fetal Intestine Small	intestine
5	chr6:54881200-54881800	Enhancers	Gastric	stomach
6	chr6:54881400-54881800	Enhancers	Stomach Mucosa	stomach
7	chr6:54881600-54882000	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr6:54881600-54882000	Enhancers	Small Intestine	intestine
9	chr6:54881600-54882400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr6:54881600-54882600	Enhancers	Duodenum Mucosa	Duodenum
11	chr6:54881600-54883000	Enhancers	Skeletal Muscle Male	skeletal muscle

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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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