Variant report

Variant rs7438033
Chromosome Location chr4:69925061-69925062
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69923800-69925400 Enhancers Stomach Mucosa stomach
2 chr4:69923800-69932400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:69924000-69925200 Enhancers Fetal Intestine Small intestine
4 chr4:69924000-69925800 Enhancers Cortex derived primary cultured neurospheres brain
5 chr4:69924400-69925400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr4:69924600-69925200 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr4:69924600-69926600 Enhancers HepG2 liver
8 chr4:69924800-69925200 Enhancers Liver Liver
9 chr4:69925000-69925800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr4:69925000-69926400 Weak transcription Pancreas Pancrea
11 chr4:69925000-69928800 Weak transcription Fetal Kidney kidney
12 chr4:69925000-69930000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr4:69925000-69932600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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