Variant report

Variant	rs17267435
Chromosome Location	chr1:211272814-211272815
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211256400-211285400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:211256800-211276600	Weak transcription	Brain Angular Gyrus	brain
3	chr1:211256800-211277000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr1:211256800-211282400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr1:211263400-211273000	Weak transcription	HSMMtube	muscle
6	chr1:211264400-211277400	Weak transcription	Brain Anterior Caudate	brain
7	chr1:211265400-211277200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr1:211266400-211280200	Weak transcription	Pancreas	Pancrea
9	chr1:211269800-211278600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:211271400-211286000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:211271800-211273200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:211271800-211273200	Weak transcription	HSMM	muscle
13	chr1:211272000-211273200	Enhancers	Adipose Nuclei	Adipose
14	chr1:211272800-211273000	Enhancers	Brain Hippocampus Middle	brain
15	chr1:211272800-211273200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:211272800-211273200	Enhancers	A549	lung
17	chr1:211272800-211276000	Enhancers	Fetal Muscle Leg	muscle

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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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