Variant report

Variant rs9811691
Chromosome Location chr3:111766124-111766125
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:111757600-111767800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr3:111760600-111766600 Weak transcription iPS-20b Cell Line embryonic stem cell
3 chr3:111760600-111767600 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr3:111760600-111767600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr3:111762400-111771000 Weak transcription Gastric stomach
6 chr3:111762600-111767800 Weak transcription Fetal Intestine Large intestine
7 chr3:111763000-111766400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr3:111763000-111767400 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr3:111763000-111767600 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr3:111763200-111766600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr3:111763200-111767600 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr3:111763200-111772800 Weak transcription Thymus Thymus
13 chr3:111763400-111769600 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
14 chr3:111765600-111766400 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr3:111765600-111766600 Enhancers HMEC breast
16 chr3:111765600-111766800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr3:111765800-111766200 Enhancers NH-A brain

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