Variant report

Variant rs10821426
Chromosome Location chr9:93185807-93185808
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93181200-93195200 Weak transcription HUES64 Cell Line embryonic stem cell
2 chr9:93182000-93195000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr9:93182200-93194800 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr9:93182200-93195000 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr9:93183200-93186200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr9:93184800-93186000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:93185400-93186000 Flanking Active TSS A549 lung
8 chr9:93185400-93186200 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr9:93185600-93186200 Enhancers HUES6 Cell Line embryonic stem cell
10 chr9:93185600-93186200 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr9:93185600-93186400 Enhancers ES-WA7 Cell Line embryonic stem cell
12 chr9:93185600-93186400 Enhancers Rectal Mucosa Donor 29 rectum
13 chr9:93185600-93186600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr9:93185600-93186600 Enhancers Fetal Intestine Large intestine
15 chr9:93185800-93186200 Bivalent Enhancer Small Intestine intestine
16 chr9:93185800-93186400 Enhancers Fetal Intestine Small intestine

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