Variant report

Variant rs4720622
Chromosome Location chr7:47918702-47918703
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:47903200-47922400 Weak transcription Adipose Nuclei Adipose
2 chr7:47903200-47923800 Weak transcription Skeletal Muscle Male skeletal muscle
3 chr7:47903400-47945000 Weak transcription Brain Angular Gyrus brain
4 chr7:47906200-47923000 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr7:47913600-47929600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr7:47916400-47949000 Weak transcription Right Ventricle heart
7 chr7:47918000-47918800 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr7:47918000-47918800 Enhancers Fetal Heart heart
9 chr7:47918200-47918800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr7:47918200-47918800 Enhancers Primary mononuclear cells fromperipheralblood Blood
11 chr7:47918200-47935200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
12 chr7:47918400-47918800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr7:47918400-47926600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr7:47918400-47926800 Weak transcription Brain Inferior Temporal Lobe brain
15 chr7:47918600-47918800 Genic enhancers Left Ventricle heart
16 chr7:47918600-47922400 Weak transcription Right Atrium heart

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