Variant report

Variant rs68192782
Chromosome Location chr1:59035247-59035248
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59033800-59035400 Enhancers NHEK skin
2 chr1:59033800-59039800 Weak transcription Placenta Amnion Placenta Amnion
3 chr1:59034200-59036200 Enhancers GM12878-XiMat blood
4 chr1:59034400-59036000 Weak transcription Esophagus oesophagus
5 chr1:59034400-59037400 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr1:59034400-59039400 Weak transcription H1 Cell Line embryonic stem cell
7 chr1:59034600-59039000 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr1:59034600-59039800 Enhancers Stomach Mucosa stomach
9 chr1:59034800-59035800 Weak transcription HMEC breast
10 chr1:59034800-59038400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr1:59035000-59036000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:59035000-59038200 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr1:59035000-59038600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr1:59035000-59039800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
15 chr1:59035200-59037000 Weak transcription H9 Cell Line embryonic stem cell

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