Variant report

Variant rs376360577
Chromosome Location chr14:105591256-105591257
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 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 chr14:105590800-105591400 Bivalent Enhancer Primary T cells fromperipheralblood blood
5 chr14:105590800-105591400 Enhancers Primary T helper cells fromperipheralblood blood
6 chr14:105590800-105591400 Bivalent Enhancer Fetal Muscle Trunk muscle
7 chr14:105590800-105591400 Enhancers Placenta Placenta
8 chr14:105590800-105591600 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr14:105590800-105593000 Enhancers Fetal Intestine Large intestine
10 chr14:105591000-105591400 Bivalent Enhancer Primary T helper 17 cells PMA-I stimulated --
11 chr14:105591000-105591400 Flanking Active TSS Duodenum Mucosa Duodenum
12 chr14:105591000-105591600 Enhancers Primary T cells from cord blood blood
13 chr14:105591000-105591600 Enhancers Primary T helper naive cells from peripheral blood blood
14 chr14:105591000-105591600 Enhancers Primary mononuclear cells fromperipheralblood Blood
15 chr14:105591200-105591400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
16 chr14:105591200-105591400 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
17 chr14:105591200-105591400 Flanking Bivalent TSS/Enh HepG2 liver
18 chr14:105591200-105591400 Bivalent Enhancer HSMMtube muscle
19 chr14:105591200-105591600 Enhancers Fetal Thymus thymus
20 chr14:105591200-105592000 Enhancers Fetal Intestine Small intestine

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