Variant report

Variant	rs192371904
Chromosome Location	chr11:121055520-121055521
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3452186	chr11:121053973-121057504	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
2	esv3393010	chr11:121054942-121057940	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
3	esv3400342	chr11:121054942-121057940	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121051200-121056200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr11:121052800-121065600	Weak transcription	Gastric	stomach
3	chr11:121053400-121057600	Weak transcription	Aorta	Aorta
4	chr11:121053800-121065600	Weak transcription	Pancreas	Pancrea
5	chr11:121054400-121061800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr11:121055400-121065600	Weak transcription	Ovary	ovary

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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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