Variant report

Variant	rs4951703
Chromosome Location	chr1:211186721-211186722
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211180600-211187000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:211181800-211193800	Weak transcription	Brain Anterior Caudate	brain
3	chr1:211182800-211228600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:211184800-211198600	Weak transcription	Brain Hippocampus Middle	brain
5	chr1:211185200-211194000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:211185400-211191800	Weak transcription	HSMMtube	muscle
7	chr1:211186400-211187200	Enhancers	NHDF-Ad	bronchial
8	chr1:211186600-211187400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:211186600-211187400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:211186600-211187400	Enhancers	Osteobl	bone
11	chr1:211186600-211189600	Genic enhancers	HSMM	muscle

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

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