Variant report

Variant	rs35867476
Chromosome Location	chr6:37186513-37186514
allele	A/G
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	chr6:37176200-37189800	Weak transcription	Thymus	Thymus
2	chr6:37184600-37189600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:37184800-37189800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:37185000-37187600	Weak transcription	NHEK	skin
5	chr6:37185400-37187000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr6:37185400-37189600	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr6:37185600-37187000	Strong transcription	Dnd41	blood
8	chr6:37185800-37186600	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr6:37185800-37189600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr6:37186200-37189600	Weak transcription	A549	lung
11	chr6:37186400-37186800	Enhancers	Fetal Thymus	thymus
12	chr6:37186400-37187000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:37186400-37187000	Enhancers	K562	blood
14	chr6:37186400-37187200	Enhancers	Primary hematopoietic stem cells	blood
15	chr6:37186400-37187200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:37186400-37189400	Weak transcription	Primary B cells from cord blood	blood

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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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