Variant report

Variant rs10028997
Chromosome Location chr4:10303703-10303704
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:10299000-10304800 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr4:10299600-10306800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr4:10299800-10305400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr4:10301000-10303800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr4:10301200-10304000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr4:10301200-10304000 Enhancers HUES48 Cell Line embryonic stem cell
7 chr4:10301200-10304000 Weak transcription Placenta Placenta
8 chr4:10301600-10303800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr4:10302000-10305800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr4:10303400-10304400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr4:10303400-10304600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr4:10303400-10304600 Enhancers HMEC breast
13 chr4:10303600-10304200 Enhancers NHEK skin

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