Variant report

Variant rs566530033
Chromosome Location chr14:105021091-105021092
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105019200-105026600 Enhancers Fetal Brain Male brain
2 chr14:105019600-105023000 Enhancers Brain Germinal Matrix brain
3 chr14:105019600-105023400 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr14:105019800-105022200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr14:105020000-105022800 Enhancers Fetal Lung lung
6 chr14:105020400-105021200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr14:105020400-105021600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
8 chr14:105020400-105022800 Bivalent Enhancer Fetal Stomach stomach
9 chr14:105020600-105021200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
10 chr14:105020600-105022400 Enhancers Cortex derived primary cultured neurospheres brain
11 chr14:105020600-105022400 Enhancers Fetal Brain Female brain
12 chr14:105020800-105021200 Bivalent Enhancer Brain Inferior Temporal Lobe brain
13 chr14:105020800-105021200 Bivalent Enhancer Placenta Placenta
14 chr14:105021000-105021400 Enhancers Brain Hippocampus Middle brain
15 chr14:105021000-105021800 Enhancers Fetal Intestine Small intestine
16 chr14:105021000-105022600 Enhancers Fetal Muscle Leg muscle
17 chr14:105021000-105029600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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