Variant report

Variant rs16904042
Chromosome Location chr8:130374938-130374939
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130365800-130377400 Weak transcription Dnd41 blood
2 chr8:130369400-130383800 Strong transcription K562 blood
3 chr8:130372200-130375600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr8:130373000-130375000 Weak transcription Fetal Thymus thymus
5 chr8:130374600-130375400 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr8:130374800-130375000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
7 chr8:130374800-130375200 Enhancers HUES48 Cell Line embryonic stem cell
8 chr8:130374800-130375400 Enhancers ES-WA7 Cell Line embryonic stem cell
9 chr8:130374800-130375400 Enhancers HUES64 Cell Line embryonic stem cell
10 chr8:130374800-130375400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr8:130374800-130375600 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr8:130374800-130375600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr8:130374800-130377200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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