Variant report

Variant rs7676752
Chromosome Location chr4:101789422-101789423
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:101786600-101796800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr4:101789200-101789800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:101789200-101789800 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
4 chr4:101789200-101789800 Enhancers HUES6 Cell Line embryonic stem cell
5 chr4:101789200-101789800 Active TSS Pancreas Pancrea
6 chr4:101789200-101789800 Enhancers Stomach Mucosa stomach
7 chr4:101789200-101790000 Enhancers Fetal Thymus thymus
8 chr4:101789200-101790000 Enhancers Dnd41 blood
9 chr4:101789200-101791400 Enhancers Fetal Intestine Small intestine
10 chr4:101789400-101789800 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr4:101789400-101789800 Enhancers HUES64 Cell Line embryonic stem cell
12 chr4:101789400-101790000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr4:101789400-101790000 Enhancers iPS-15b Cell Line embryonic stem cell

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