Variant report

Variant rs2838317
Chromosome Location chr21:44991791-44991792
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:44980400-44998400 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr21:44983000-44991800 Weak transcription Placenta Amnion Placenta Amnion
3 chr21:44983000-44993400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr21:44987200-44994600 Weak transcription Spleen Spleen
5 chr21:44987200-45005000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr21:44987200-45005000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr21:44988000-44993800 Enhancers Fetal Muscle Leg muscle
8 chr21:44988200-44993200 Enhancers HSMM muscle
9 chr21:44988800-44994000 Enhancers Fetal Brain Male brain
10 chr21:44988800-44996600 Enhancers HSMMtube muscle
11 chr21:44989000-44992000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr21:44989000-44998000 Weak transcription Gastric stomach
13 chr21:44990200-44992400 Enhancers HepG2 liver
14 chr21:44990600-44992200 Weak transcription Muscle Satellite Cultured Cells --
15 chr21:44990600-44992200 Weak transcription Fetal Stomach stomach
16 chr21:44990600-44994400 Weak transcription Colon Smooth Muscle Colon
17 chr21:44991000-44993000 Enhancers Fetal Muscle Trunk muscle
18 chr21:44991200-44991800 Enhancers Adipose Nuclei Adipose
19 chr21:44991200-44992000 Weak transcription Fetal Brain Female brain
20 chr21:44991400-44992600 Enhancers Skeletal Muscle Female skeletal muscle

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