Variant report

Variant rs16904101
Chromosome Location chr8:130524638-130524639
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130521200-130526600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr8:130521400-130526200 Weak transcription NH-A brain
3 chr8:130521400-130526400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr8:130521400-130526400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr8:130521400-130526400 Weak transcription HSMM muscle
6 chr8:130521400-130526400 Weak transcription Osteobl bone
7 chr8:130521400-130526600 Weak transcription Muscle Satellite Cultured Cells --
8 chr8:130522200-130526000 Weak transcription NHEK skin
9 chr8:130522200-130526200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr8:130522400-130526200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr8:130523000-130526000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr8:130523000-130526200 Weak transcription HMEC breast
13 chr8:130523800-130527000 Enhancers Fetal Intestine Small intestine
14 chr8:130523800-130528000 Enhancers Fetal Intestine Large intestine
15 chr8:130524200-130526200 Weak transcription Fetal Heart heart
16 chr8:130524200-130526400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
17 chr8:130524200-130527600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
18 chr8:130524600-130525600 Weak transcription HUES64 Cell Line embryonic stem cell
19 chr8:130524600-130526200 Strong transcription K562 blood
20 chr8:130524600-130526400 Weak transcription Dnd41 blood

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