Variant report

Variant rs73094304
Chromosome Location chr4:18399422-18399423
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:18391600-18404800 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr4:18393400-18403000 Weak transcription Small Intestine intestine
3 chr4:18396600-18400600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr4:18396800-18403000 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr4:18399000-18401800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr4:18399200-18399800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr4:18399200-18400400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr4:18399200-18401000 Enhancers HUES64 Cell Line embryonic stem cell
9 chr4:18399200-18401000 Enhancers Fetal Intestine Large intestine
10 chr4:18399200-18401000 Enhancers Fetal Intestine Small intestine
11 chr4:18399200-18401200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr4:18399400-18399600 Enhancers Fetal Brain Male brain
13 chr4:18399400-18400200 Enhancers Placenta Amnion Placenta Amnion
14 chr4:18399400-18400600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
15 chr4:18399400-18400800 Enhancers iPS-18 Cell Line embryonic stem cell
16 chr4:18399400-18401800 Enhancers Brain Germinal Matrix brain

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