Variant report

Variant rs35992537
Chromosome Location chr19:41509201-41509202
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41505600-41509400 Enhancers Fetal Intestine Small intestine
2 chr19:41506600-41509400 Weak transcription A549 lung
3 chr19:41507400-41529200 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr19:41508000-41511800 Strong transcription Liver Liver
5 chr19:41508000-41522400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr19:41508200-41509400 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr19:41509000-41510400 Enhancers Fetal Intestine Large intestine
8 chr19:41509200-41509400 Enhancers Rectal Mucosa Donor 29 rectum
9 chr19:41509200-41509600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr19:41509200-41509800 Enhancers HUES48 Cell Line embryonic stem cell
11 chr19:41509200-41509800 Enhancers HUES6 Cell Line embryonic stem cell
12 chr19:41509200-41510400 Enhancers ES-I3 Cell Line embryonic stem cell

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