Variant report

Variant	rs6938117
Chromosome Location	chr6:15923849-15923850
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	chr6:15920200-15924600	Enhancers	Placenta	Placenta
2	chr6:15921400-15924000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:15921600-15924200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:15921600-15924400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:15921600-15927600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:15921600-15929400	Weak transcription	Adipose Nuclei	Adipose
7	chr6:15922000-15924200	Enhancers	Placenta Amnion	Placenta Amnion
8	chr6:15922000-15924400	Enhancers	HUVEC	blood vessel
9	chr6:15922000-15926600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr6:15922200-15924400	Enhancers	K562	blood
11	chr6:15922600-15924000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr6:15922600-15925200	Enhancers	Fetal Muscle Leg	muscle
13	chr6:15923200-15924000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:15923200-15924000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:15923600-15924000	Enhancers	Brain Hippocampus Middle	brain
16	chr6:15923600-15926600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr6:15923800-15925800	Weak transcription	Aorta	Aorta

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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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