Variant report

Variant rs4983430
Chromosome Location chr14:105033619-105033620
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105030400-105040400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr14:105030800-105033800 Weak transcription Fetal Brain Female brain
3 chr14:105030800-105036600 Weak transcription Fetal Heart heart
4 chr14:105031000-105038600 Weak transcription Right Atrium heart
5 chr14:105031400-105035600 Weak transcription Brain Germinal Matrix brain
6 chr14:105033200-105034200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
7 chr14:105033400-105033800 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
8 chr14:105033400-105034000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr14:105033400-105034400 Bivalent Enhancer Fetal Stomach stomach
10 chr14:105033400-105046000 Bivalent Enhancer Fetal Muscle Trunk muscle
11 chr14:105033600-105034000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr14:105033600-105034200 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
13 chr14:105033600-105034200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
14 chr14:105033600-105034200 Enhancers Fetal Lung lung
15 chr14:105033600-105034200 Enhancers A549 lung
16 chr14:105033600-105034600 Enhancers Fetal Brain Male brain
17 chr14:105033600-105034600 Bivalent Enhancer Fetal Muscle Leg muscle

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