Variant report

Variant rs1980265
Chromosome Location chr6:44928868-44928869
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:44913400-44930000 Weak transcription Pancreas Pancrea
2 chr6:44915400-44932800 Weak transcription Left Ventricle heart
3 chr6:44919600-44943200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
4 chr6:44920600-44937600 Weak transcription Primary hematopoietic stem cells blood
5 chr6:44923400-44935000 Weak transcription Fetal Adrenal Gland Adrenal Gland
6 chr6:44927400-44930400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr6:44928400-44929000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr6:44928400-44929200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr6:44928400-44930800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr6:44928600-44929000 Enhancers GM12878-XiMat blood
11 chr6:44928600-44929000 Enhancers NHDF-Ad bronchial
12 chr6:44928600-44929000 Enhancers NHLF lung
13 chr6:44928600-44929200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr6:44928600-44929200 Enhancers HepG2 liver
15 chr6:44928800-44929200 Weak transcription Primary B cells from cord blood blood
16 chr6:44928800-44933800 Weak transcription Muscle Satellite Cultured Cells --

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