Variant report

Variant rs34674329
Chromosome Location chr4:101789903-101789904
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr4:101789200-101790000 Enhancers Fetal Thymus thymus
3 chr4:101789200-101790000 Enhancers Dnd41 blood
4 chr4:101789200-101791400 Enhancers Fetal Intestine Small intestine
5 chr4:101789400-101790000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr4:101789400-101790000 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr4:101789600-101790000 Enhancers Esophagus oesophagus
8 chr4:101789800-101790000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr4:101789800-101790200 Enhancers Fetal Intestine Large intestine
10 chr4:101789800-101790800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr4:101789800-101792400 Weak transcription Pancreas Pancrea
12 chr4:101789800-101794200 Weak transcription HUES6 Cell Line embryonic stem cell

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