Variant report

Variant	rs550392787
Chromosome Location	chr11:83190418-83190419
allele	-/G
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	esv2249153	chr11:83190418-83190419	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83183600-83192000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr11:83183800-83191000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:83183800-83191200	Weak transcription	Brain Hippocampus Middle	brain
4	chr11:83187200-83196600	Weak transcription	Brain Substantia Nigra	brain
5	chr11:83187400-83191200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr11:83187400-83191200	Weak transcription	Brain Anterior Caudate	brain
7	chr11:83187400-83191400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:83187400-83191400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr11:83187400-83191400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr11:83187600-83191400	Weak transcription	Brain Angular Gyrus	brain
11	chr11:83187600-83191600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:83188800-83192600	Weak transcription	Pancreatic Islets	Pancreatic Islet

Quick Search:

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

what's new

Quick links