Variant report

Variant	rs12142635
Chromosome Location	chr1:226976332-226976333
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226966600-226986400	Weak transcription	Right Atrium	heart
2	chr1:226969600-226976400	Enhancers	Brain Cingulate Gyrus	brain
3	chr1:226970800-226977000	Enhancers	Rectal Smooth Muscle	rectum
4	chr1:226971000-226976400	Enhancers	Colon Smooth Muscle	Colon
5	chr1:226971200-226976400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr1:226971600-226986800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:226972200-226976600	Enhancers	Stomach Smooth Muscle	stomach
8	chr1:226974200-226976400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:226974200-226976400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:226974400-226976400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:226975200-226976600	Enhancers	GM12878-XiMat	blood
12	chr1:226976000-226976400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:226976000-226976400	Enhancers	Brain Angular Gyrus	brain
14	chr1:226976200-226976400	Enhancers	Brain Hippocampus Middle	brain
15	chr1:226976200-226976400	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr1:226976200-226976400	Enhancers	NHEK	skin

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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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