Variant report

Variant rs4798721
Chromosome Location chr18:8936309-8936310
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:8929200-8942800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr18:8931600-8937200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr18:8932200-8937000 Weak transcription H9 Cell Line embryonic stem cell
4 chr18:8933400-8936800 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr18:8933800-8937000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr18:8934200-8937000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr18:8934200-8937000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr18:8934200-8943200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr18:8935000-8937200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr18:8935200-8936800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr18:8936000-8937600 Enhancers Stomach Mucosa stomach
12 chr18:8936000-8939200 Enhancers Placenta Placenta
13 chr18:8936000-8939600 Enhancers Placenta Amnion Placenta Amnion
14 chr18:8936200-8937800 Enhancers Fetal Intestine Small intestine
15 chr18:8936200-8938200 Enhancers Fetal Intestine Large intestine
16 chr18:8936200-8938400 Enhancers Fetal Kidney kidney
17 chr18:8936200-8939800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
18 chr18:8936200-8940800 Enhancers K562 blood

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