Variant report

Variant rs35818159
Chromosome Location chr2:191409616-191409617
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:191403000-191416800 Weak transcription Gastric stomach
2 chr2:191405400-191409800 Weak transcription Aorta Aorta
3 chr2:191405400-191416800 Weak transcription Esophagus oesophagus
4 chr2:191406600-191410000 Weak transcription Duodenum Smooth Muscle Duodenum
5 chr2:191407000-191410200 Weak transcription Brain Anterior Caudate brain
6 chr2:191407600-191409800 Enhancers Osteobl bone
7 chr2:191408200-191410000 Weak transcription Right Atrium heart
8 chr2:191408400-191411600 Weak transcription Psoas Muscle Psoas
9 chr2:191408800-191410000 Weak transcription Muscle Satellite Cultured Cells --
10 chr2:191409000-191410000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr2:191409000-191410200 Weak transcription HSMM muscle
12 chr2:191409400-191413600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr2:191409600-191409800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr2:191409600-191409800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr2:191409600-191409800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr2:191409600-191409800 Enhancers NHLF lung

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