Variant report

Variant rs38432
Chromosome Location chr7:30552300-30552301
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:30545000-30584600 Weak transcription Aorta Aorta
2 chr7:30545200-30556800 Weak transcription Pancreas Pancrea
3 chr7:30545200-30559800 Weak transcription Primary neutrophils fromperipheralblood blood
4 chr7:30545200-30562200 Weak transcription Small Intestine intestine
5 chr7:30545200-30587600 Weak transcription HSMMtube muscle
6 chr7:30545400-30559600 Weak transcription Monocytes-CD14+_RO01746 blood
7 chr7:30545400-30560200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr7:30545400-30560600 Weak transcription Brain Substantia Nigra brain
9 chr7:30545400-30560600 Weak transcription Colon Smooth Muscle Colon
10 chr7:30545400-30576200 Weak transcription Stomach Smooth Muscle stomach
11 chr7:30545400-30576600 Weak transcription Primary T helper cells fromperipheralblood blood
12 chr7:30545600-30586200 Weak transcription Brain Anterior Caudate brain
13 chr7:30550600-30553600 Weak transcription Adipose Nuclei Adipose
14 chr7:30550600-30553600 Weak transcription Placenta Placenta
15 chr7:30550600-30559600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr7:30550600-30559600 Weak transcription Primary monocytes fromperipheralblood blood
17 chr7:30551200-30554000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
18 chr7:30551400-30555600 Weak transcription Lung lung
19 chr7:30551800-30552600 Weak transcription Fetal Intestine Small intestine
20 chr7:30552200-30553200 Enhancers Fetal Intestine Large intestine
21 chr7:30552200-30559800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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