Variant report

Variant rs139321182
Chromosome Location chr6:12770388-12770389
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:12762200-12780600 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr6:12766400-12770600 Weak transcription Aorta Aorta
3 chr6:12769400-12770400 Enhancers Brain Germinal Matrix brain
4 chr6:12769400-12773800 Enhancers Fetal Brain Female brain
5 chr6:12769600-12770600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr6:12769600-12770600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
7 chr6:12769600-12770800 Enhancers HSMM muscle
8 chr6:12769600-12774000 Enhancers Fetal Brain Male brain
9 chr6:12769800-12770400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr6:12770000-12770400 Enhancers Brain Inferior Temporal Lobe brain
11 chr6:12770000-12770600 Enhancers HSMMtube muscle
12 chr6:12770200-12770600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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