Variant report

Variant rs117075418
Chromosome Location chr14:105591563-105591564
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105588000-105592800 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr14:105590400-105602600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr14:105590600-105591800 Enhancers Primary hematopoietic stem cells blood
4 chr14:105590800-105591600 Bivalent Enhancer Fetal Muscle Leg muscle
5 chr14:105590800-105593000 Enhancers Fetal Intestine Large intestine
6 chr14:105591000-105591600 Enhancers Primary T cells from cord blood blood
7 chr14:105591000-105591600 Enhancers Primary T helper naive cells from peripheral blood blood
8 chr14:105591000-105591600 Enhancers Primary mononuclear cells fromperipheralblood Blood
9 chr14:105591200-105591600 Enhancers Fetal Thymus thymus
10 chr14:105591200-105592000 Enhancers Fetal Intestine Small intestine
11 chr14:105591400-105591600 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
12 chr14:105591400-105591600 Bivalent Enhancer HepG2 liver
13 chr14:105591400-105591800 Enhancers Duodenum Mucosa Duodenum

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