Variant report

Variant rs12321819
Chromosome Location chr12:49941997-49941998
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:49933000-49942600 Weak transcription Pancreas Pancrea
2 chr12:49933400-49942000 Weak transcription Right Ventricle heart
3 chr12:49933400-49942400 Weak transcription Right Atrium heart
4 chr12:49934200-49942000 Weak transcription Brain Inferior Temporal Lobe brain
5 chr12:49934600-49942200 Weak transcription Brain Angular Gyrus brain
6 chr12:49937400-49942000 Weak transcription Primary T killer naive cells fromperipheralblood blood
7 chr12:49938800-49942400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr12:49940200-49942600 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr12:49940400-49942600 Bivalent Enhancer NHEK skin
10 chr12:49940400-49943000 Enhancers HMEC breast
11 chr12:49941000-49942200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr12:49941000-49942400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr12:49941400-49942600 Enhancers HepG2 liver
14 chr12:49941400-49942800 Enhancers Spleen Spleen
15 chr12:49941600-49942000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
16 chr12:49941600-49942200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr12:49941600-49942800 Bivalent Enhancer Esophagus oesophagus
18 chr12:49941800-49942400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
19 chr12:49941800-49942400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
20 chr12:49941800-49942600 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
21 chr12:49941800-49942800 Bivalent Enhancer Fetal Brain Male brain
22 chr12:49941800-49942800 Enhancers Gastric stomach

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