Variant report

Variant rs7661016
Chromosome Location chr4:189139730-189139731
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:189137800-189140000 Enhancers Fetal Brain Male brain
2 chr4:189139200-189139800 Active TSS H9 Cell Line embryonic stem cell
3 chr4:189139200-189139800 Active TSS iPS-20b Cell Line embryonic stem cell
4 chr4:189139200-189140200 Active TSS ES-I3 Cell Line embryonic stem cell
5 chr4:189139200-189140200 Active TSS iPS-15b Cell Line embryonic stem cell
6 chr4:189139400-189139800 Active TSS H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr4:189139400-189139800 Active TSS HUES64 Cell Line embryonic stem cell
8 chr4:189139400-189139800 Active TSS iPS-18 Cell Line embryonic stem cell
9 chr4:189139400-189139800 Active TSS ES-UCSF4 Cell Line embryonic stem cell
10 chr4:189139400-189139800 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr4:189139400-189140000 Active TSS H1 Cell Line embryonic stem cell
12 chr4:189139400-189140000 Active TSS HUES48 Cell Line embryonic stem cell
13 chr4:189139400-189140000 Enhancers Fetal Stomach stomach
14 chr4:189139600-189139800 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
15 chr4:189139600-189139800 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle
16 chr4:189139600-189140000 Active TSS HUES6 Cell Line embryonic stem cell
17 chr4:189139600-189140200 Bivalent Enhancer Placenta Placenta

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