Variant report

Variant rs10135029
Chromosome Location chr14:105117810-105117811
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105116800-105118000 Enhancers Primary B cells from cord blood blood
2 chr14:105116800-105118000 Enhancers Primary hematopoietic stem cells short term culture blood
3 chr14:105116800-105118000 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
4 chr14:105116800-105118600 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr14:105116800-105120600 Weak transcription Brain Angular Gyrus brain
6 chr14:105116800-105125800 Weak transcription ES-WA7 Cell Line embryonic stem cell
7 chr14:105116800-105125800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr14:105116800-105131600 Weak transcription Right Atrium heart
9 chr14:105117000-105118000 Enhancers Primary B cells from peripheral blood blood
10 chr14:105117000-105118000 Enhancers Brain Cingulate Gyrus brain
11 chr14:105117200-105118200 Weak transcription Liver Liver
12 chr14:105117200-105123200 Weak transcription Brain Hippocampus Middle brain
13 chr14:105117400-105120000 Weak transcription Pancreas Pancrea
14 chr14:105117400-105120400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr14:105117600-105118200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
16 chr14:105117600-105118400 Weak transcription Spleen Spleen
17 chr14:105117800-105120800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell

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