Variant report

Variant rs1096028
Chromosome Location chr12:51222501-51222502
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr12:51213400-51222600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr12:51213800-51222800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr12:51218800-51223400 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr12:51219200-51223000 Weak transcription Brain Anterior Caudate brain
7 chr12:51219600-51222800 Weak transcription Thymus Thymus
8 chr12:51221800-51222600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:51221800-51222600 Enhancers HMEC breast
10 chr12:51222000-51223000 Enhancers Esophagus oesophagus
11 chr12:51222200-51222800 Weak transcription Brain Cingulate Gyrus brain
12 chr12:51222200-51223200 Enhancers Fetal Muscle Leg muscle
13 chr12:51222200-51223200 Enhancers Skeletal Muscle Male skeletal muscle
14 chr12:51222200-51223400 Enhancers Fetal Muscle Trunk muscle
15 chr12:51222400-51223000 Enhancers Brain Substantia Nigra brain
16 chr12:51222400-51223200 Enhancers Skeletal Muscle Female skeletal muscle
17 chr12:51222400-51223400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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