Variant report

Variant rs73101856
Chromosome Location chr1:220705094-220705095
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220702600-220706400 Active TSS Fetal Brain Female brain
2 chr1:220703000-220705600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr1:220703400-220706800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr1:220703400-220724400 Weak transcription Aorta Aorta
5 chr1:220703600-220705600 Weak transcription H1 Cell Line embryonic stem cell
6 chr1:220704000-220707800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:220704200-220705800 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr1:220704200-220705800 Enhancers Pancreatic Islets Pancreatic Islet
9 chr1:220704400-220705600 Weak transcription Adipose Nuclei Adipose
10 chr1:220704400-220707600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:220704600-220705200 Enhancers Cortex derived primary cultured neurospheres brain
12 chr1:220704600-220705600 Weak transcription Fetal Heart heart
13 chr1:220704600-220706200 Enhancers Brain Germinal Matrix brain
14 chr1:220704600-220710000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:220705000-220705200 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
16 chr1:220705000-220705800 Enhancers iPS-20b Cell Line embryonic stem cell
17 chr1:220705000-220705800 Weak transcription Fetal Brain Male brain

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