Variant report

Variant rs45579537
Chromosome Location chr4:3446284-3446285
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3436600-3449000 Weak transcription Fetal Brain Female brain
2 chr4:3437000-3450000 Weak transcription Brain Germinal Matrix brain
3 chr4:3437200-3451200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr4:3438000-3448000 Weak transcription Right Ventricle heart
5 chr4:3443000-3446600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr4:3443200-3450600 Weak transcription Esophagus oesophagus
7 chr4:3443200-3451400 Weak transcription Fetal Lung lung
8 chr4:3444600-3446400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr4:3445400-3446400 Enhancers Gastric stomach
10 chr4:3445400-3448200 Weak transcription Fetal Intestine Small intestine
11 chr4:3445600-3446400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr4:3445600-3447800 Weak transcription Spleen Spleen
13 chr4:3445600-3448200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr4:3445600-3449200 Weak transcription Pancreas Pancrea
15 chr4:3445600-3451600 Weak transcription Primary hematopoietic stem cells short term culture blood
16 chr4:3445800-3451200 Weak transcription HepG2 liver
17 chr4:3445800-3453600 Weak transcription Skeletal Muscle Female skeletal muscle
18 chr4:3446200-3446600 Weak transcription Liver Liver

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