Variant report

Variant rs10173975
Chromosome Location chr2:191411368-191411369
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:191403000-191416800 Weak transcription Gastric stomach
2 chr2:191405400-191416800 Weak transcription Esophagus oesophagus
3 chr2:191408400-191411600 Weak transcription Psoas Muscle Psoas
4 chr2:191409400-191413600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:191410400-191414000 Weak transcription NHLF lung
6 chr2:191410600-191411400 Weak transcription HMEC breast
7 chr2:191410600-191411400 Enhancers Osteobl bone
8 chr2:191410600-191411600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:191410600-191411600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:191410600-191411800 Enhancers A549 lung
11 chr2:191410600-191412800 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr2:191410800-191412600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr2:191410800-191418200 Weak transcription Pancreatic Islets Pancreatic Islet
14 chr2:191411000-191411400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
15 chr2:191411000-191411800 Enhancers Brain Anterior Caudate brain
16 chr2:191411000-191443000 Weak transcription Right Atrium heart
17 chr2:191411200-191411800 Enhancers Fetal Intestine Large intestine

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