Variant report

Variant rs10234443
Chromosome Location chr7:121442884-121442885
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:121436400-121444000 Enhancers NHEK skin
2 chr7:121439200-121444000 Enhancers Cortex derived primary cultured neurospheres brain
3 chr7:121439600-121443800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr7:121440200-121443800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr7:121440600-121450400 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr7:121441600-121443200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr7:121441600-121443400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr7:121441800-121443200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr7:121442400-121443200 Weak transcription HMEC breast
10 chr7:121442600-121443000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr7:121442600-121443800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:121442800-121443200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr7:121442800-121443200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr7:121442800-121443400 Enhancers Fetal Brain Female brain

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