Variant report

Variant rs921777
Chromosome Location chr8:2774638-2774639
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:2772200-2777400 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr8:2772200-2779600 Weak transcription Gastric stomach
3 chr8:2772400-2779800 Weak transcription Fetal Stomach stomach
4 chr8:2773400-2774800 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr8:2773400-2775000 Enhancers HUES64 Cell Line embryonic stem cell
6 chr8:2773400-2775000 Enhancers Fetal Intestine Small intestine
7 chr8:2773400-2776000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr8:2773600-2774800 Enhancers Fetal Intestine Large intestine
9 chr8:2773600-2775400 Enhancers Muscle Satellite Cultured Cells --
10 chr8:2773600-2775400 Enhancers Osteobl bone
11 chr8:2773800-2774800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr8:2773800-2775600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr8:2774200-2776000 Weak transcription HUES48 Cell Line embryonic stem cell
14 chr8:2774200-2776800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr8:2774400-2775200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr8:2774400-2775600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr8:2774400-2777400 Weak transcription H1 Cell Line embryonic stem cell
18 chr8:2774600-2775000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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