Variant report

Variant	rs17020702
Chromosome Location	chr2:37639534-37639535
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37625600-37641800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:37638800-37639600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:37638800-37639600	Enhancers	Fetal Brain Male	brain
4	chr2:37638800-37639600	Enhancers	HSMMtube	muscle
5	chr2:37638800-37639800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:37639000-37639600	Enhancers	Fetal Brain Female	brain
7	chr2:37639000-37639800	Enhancers	HSMM	muscle
8	chr2:37639000-37640000	Enhancers	Fetal Thymus	thymus
9	chr2:37639200-37639600	Enhancers	Thymus	Thymus

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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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