Variant report

Variant rs10911822
Chromosome Location chr1:172465725-172465726
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172454200-172466000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:172460800-172466000 Weak transcription Aorta Aorta
3 chr1:172460800-172466800 Enhancers Fetal Intestine Large intestine
4 chr1:172462600-172466000 Enhancers HepG2 liver
5 chr1:172464000-172466000 Weak transcription Right Atrium heart
6 chr1:172464200-172466800 Enhancers K562 blood
7 chr1:172464600-172466800 Enhancers Fetal Intestine Small intestine
8 chr1:172464800-172466200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr1:172464800-172467200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr1:172464800-172471000 Enhancers Placenta Amnion Placenta Amnion
11 chr1:172465000-172466200 Enhancers Duodenum Mucosa Duodenum
12 chr1:172465000-172467000 Enhancers Stomach Mucosa stomach
13 chr1:172465000-172467800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr1:172465000-172468600 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr1:172465200-172466000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr1:172465200-172466400 Weak transcription Pancreas Pancrea
17 chr1:172465600-172466200 Enhancers Esophagus oesophagus
18 chr1:172465600-172466800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
19 chr1:172465600-172470000 Enhancers Primary monocytes fromperipheralblood blood

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