Variant report

Variant rs185919613
Chromosome Location chr6:150612019-150612020
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150604200-150617000 Weak transcription Pancreas Pancrea
2 chr6:150610200-150612200 Enhancers K562 blood
3 chr6:150610800-150612200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr6:150610800-150612200 Enhancers HMEC breast
5 chr6:150610800-150612400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr6:150610800-150612400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:150611000-150612400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr6:150611200-150612400 Enhancers Osteobl bone
9 chr6:150611400-150612200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr6:150611400-150612200 Flanking Active TSS Muscle Satellite Cultured Cells --
11 chr6:150611400-150612200 Flanking Active TSS NHEK skin
12 chr6:150611600-150614200 Weak transcription NHDF-Ad bronchial
13 chr6:150611600-150615400 Weak transcription Esophagus oesophagus
14 chr6:150611800-150613200 Weak transcription Placenta Placenta
15 chr6:150611800-150614200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr6:150612000-150612400 Enhancers NH-A brain
17 chr6:150612000-150613400 Weak transcription Placenta Amnion Placenta Amnion
18 chr6:150612000-150614600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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