Variant report

Variant rs587598630
Chromosome Location chr14:105590980-105590981
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr14:105590200-105591200 Enhancers Colonic Mucosa Colon
3 chr14:105590400-105591000 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
4 chr14:105590400-105602600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr14:105590600-105591800 Enhancers Primary hematopoietic stem cells blood
6 chr14:105590800-105591000 Flanking Bivalent TSS/Enh IMR90 fetal lung fibroblasts Cell Line lung
7 chr14:105590800-105591000 Enhancers Duodenum Mucosa Duodenum
8 chr14:105590800-105591200 Bivalent Enhancer HepG2 liver
9 chr14:105590800-105591400 Bivalent Enhancer Primary T cells fromperipheralblood blood
10 chr14:105590800-105591400 Enhancers Primary T helper cells fromperipheralblood blood
11 chr14:105590800-105591400 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr14:105590800-105591400 Enhancers Placenta Placenta
13 chr14:105590800-105591600 Bivalent Enhancer Fetal Muscle Leg muscle
14 chr14:105590800-105593000 Enhancers Fetal Intestine Large intestine

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