Variant report

Variant rs1436611
Chromosome Location chr8:35587181-35587182
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:35575000-35587400 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr8:35575000-35600200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr8:35576000-35631600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr8:35577000-35587800 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr8:35582000-35640600 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr8:35582200-35590400 Weak transcription H9 Cell Line embryonic stem cell
7 chr8:35583200-35589200 Weak transcription Fetal Kidney kidney
8 chr8:35584400-35598000 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr8:35584600-35590400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr8:35584600-35603200 Weak transcription Fetal Brain Female brain
11 chr8:35584800-35589200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr8:35585000-35589000 Weak transcription HUES64 Cell Line embryonic stem cell
13 chr8:35585000-35590200 Weak transcription Stomach Mucosa stomach
14 chr8:35585200-35587800 Weak transcription Cortex derived primary cultured neurospheres brain
15 chr8:35585200-35590000 Weak transcription H1 Cell Line embryonic stem cell
16 chr8:35585600-35588400 Weak transcription HUES48 Cell Line embryonic stem cell
17 chr8:35585800-35587600 Enhancers Fetal Lung lung
18 chr8:35586000-35587600 Weak transcription iPS-18 Cell Line embryonic stem cell
19 chr8:35586400-35587200 Enhancers Small Intestine intestine
20 chr8:35587000-35587200 Enhancers HUES6 Cell Line embryonic stem cell
21 chr8:35587000-35590400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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