Variant report

Variant rs35647158
Chromosome Location chr14:32187571-32187572
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32165600-32188200 Weak transcription Right Ventricle heart
2 chr14:32171000-32200600 Weak transcription Placenta Amnion Placenta Amnion
3 chr14:32172000-32188200 Weak transcription Duodenum Smooth Muscle Duodenum
4 chr14:32173400-32189800 Weak transcription Primary B cells from cord blood blood
5 chr14:32173400-32218000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr14:32174600-32200000 Weak transcription Primary T helper naive cells fromperipheralblood blood
7 chr14:32175400-32193400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr14:32175400-32205600 Weak transcription Ovary ovary
9 chr14:32181400-32200600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr14:32186200-32188200 Enhancers Liver Liver
11 chr14:32186400-32188400 Enhancers Rectal Smooth Muscle rectum
12 chr14:32186400-32188600 Enhancers Fetal Heart heart
13 chr14:32186600-32187600 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr14:32186800-32205600 Weak transcription Primary T cells from cord blood blood
15 chr14:32187000-32188200 Weak transcription Psoas Muscle Psoas
16 chr14:32187200-32196000 Weak transcription Aorta Aorta
17 chr14:32187400-32188400 Enhancers Fetal Brain Female brain
18 chr14:32187400-32199000 Weak transcription HepG2 liver

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