Variant report

Variant	rs4535729
Chromosome Location	chr8:59171744-59171745
allele	C/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	chr8:59167400-59171800	Enhancers	Brain Germinal Matrix	brain
2	chr8:59167400-59172200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr8:59169000-59172200	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr8:59169400-59172000	Enhancers	Brain Cingulate Gyrus	brain
5	chr8:59170200-59172000	Enhancers	Brain Angular Gyrus	brain
6	chr8:59170200-59172000	Enhancers	Brain Substantia Nigra	brain
7	chr8:59170200-59172200	Enhancers	Brain Hippocampus Middle	brain
8	chr8:59170600-59173000	Weak transcription	GM12878-XiMat	blood
9	chr8:59170800-59172400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:59170800-59172400	Weak transcription	Fetal Muscle Leg	muscle
11	chr8:59170800-59187800	Weak transcription	Fetal Lung	lung
12	chr8:59171200-59172000	Enhancers	Brain Anterior Caudate	brain
13	chr8:59171400-59171800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:59171600-59171800	Enhancers	Left Ventricle	heart

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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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