Variant report

Variant rs2664234
Chromosome Location chr2:211395046-211395047
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:211391600-211396800 Weak transcription Fetal Intestine Small intestine
2 chr2:211392400-211396000 Weak transcription HepG2 liver
3 chr2:211393000-211397000 Weak transcription Fetal Intestine Large intestine
4 chr2:211393800-211395200 Weak transcription Liver Liver
5 chr2:211394400-211399400 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr2:211394400-211399600 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr2:211394600-211395800 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr2:211394800-211395200 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr2:211395000-211395400 Enhancers HUES48 Cell Line embryonic stem cell
10 chr2:211395000-211399200 Enhancers Breast Myoepithelial Primary Cells Breast

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