Variant report

Variant rs373502992
Chromosome Location chr14:105591054-105591055
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr14:105590400-105602600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr14:105590600-105591800 Enhancers Primary hematopoietic stem cells blood
5 chr14:105590800-105591200 Bivalent Enhancer HepG2 liver
6 chr14:105590800-105591400 Bivalent Enhancer Primary T cells fromperipheralblood blood
7 chr14:105590800-105591400 Enhancers Primary T helper cells fromperipheralblood blood
8 chr14:105590800-105591400 Bivalent Enhancer Fetal Muscle Trunk muscle
9 chr14:105590800-105591400 Enhancers Placenta Placenta
10 chr14:105590800-105591600 Bivalent Enhancer Fetal Muscle Leg muscle
11 chr14:105590800-105593000 Enhancers Fetal Intestine Large intestine
12 chr14:105591000-105591200 Bivalent/Poised TSS IMR90 fetal lung fibroblasts Cell Line lung
13 chr14:105591000-105591200 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
14 chr14:105591000-105591200 Flanking Bivalent TSS/Enh Rectal Mucosa Donor 29 rectum
15 chr14:105591000-105591400 Bivalent Enhancer Primary T helper 17 cells PMA-I stimulated --
16 chr14:105591000-105591400 Flanking Active TSS Duodenum Mucosa Duodenum
17 chr14:105591000-105591600 Enhancers Primary T cells from cord blood blood
18 chr14:105591000-105591600 Enhancers Primary T helper naive cells from peripheral blood blood
19 chr14:105591000-105591600 Enhancers Primary mononuclear cells fromperipheralblood Blood

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