Variant report

Variant rs73101861
Chromosome Location chr1:220705882-220705883
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220702600-220706400 Active TSS Fetal Brain Female brain
2 chr1:220703400-220706800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr1:220703400-220724400 Weak transcription Aorta Aorta
4 chr1:220704000-220707800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:220704400-220707600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:220704600-220706200 Enhancers Brain Germinal Matrix brain
7 chr1:220704600-220710000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:220705200-220706000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr1:220705200-220706800 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr1:220705600-220706200 Enhancers Fetal Heart heart
11 chr1:220705800-220706000 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr1:220705800-220706000 Enhancers Fetal Brain Male brain

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