Variant report

Variant	rs10178950
Chromosome Location	chr2:210449876-210449877
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210443600-210461000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:210444800-210456800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:210446200-210456800	Weak transcription	Brain Anterior Caudate	brain
4	chr2:210446600-210461600	Weak transcription	Brain Angular Gyrus	brain
5	chr2:210447800-210460400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr2:210448600-210452000	Enhancers	Fetal Brain Male	brain
7	chr2:210448800-210450400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr2:210449000-210451200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr2:210449200-210451000	Weak transcription	Brain Germinal Matrix	brain
10	chr2:210449600-210450000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr2:210449600-210450600	Weak transcription	Fetal Brain Female	brain
12	chr2:210449600-210451800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:210449800-210450000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:210449800-210451200	Strong transcription	H9 Derived Neuron 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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