Variant report

Variant rs1096029
Chromosome Location chr12:51222827-51222828
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:51205000-51228200 Weak transcription Gastric stomach
2 chr12:51210600-51223400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr12:51218800-51223400 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr12:51219200-51223000 Weak transcription Brain Anterior Caudate brain
5 chr12:51222000-51223000 Enhancers Esophagus oesophagus
6 chr12:51222200-51223200 Enhancers Fetal Muscle Leg muscle
7 chr12:51222200-51223200 Enhancers Skeletal Muscle Male skeletal muscle
8 chr12:51222200-51223400 Enhancers Fetal Muscle Trunk muscle
9 chr12:51222400-51223000 Enhancers Brain Substantia Nigra brain
10 chr12:51222400-51223200 Enhancers Skeletal Muscle Female skeletal muscle
11 chr12:51222400-51223400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr12:51222600-51223000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr12:51222800-51223000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr12:51222800-51223000 Enhancers Brain Cingulate Gyrus brain
15 chr12:51222800-51223200 Enhancers Thymus Thymus

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