Variant report

Variant rs667553
Chromosome Location chr1:61394561-61394562
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:61386600-61402400 Weak transcription H1 Cell Line embryonic stem cell
2 chr1:61387400-61395800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr1:61387400-61408200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr1:61388200-61408000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr1:61389400-61396000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr1:61389600-61396600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:61391400-61402000 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr1:61391400-61402400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:61391400-61408000 Weak transcription H9 Cell Line embryonic stem cell
10 chr1:61391600-61395400 Weak transcription Fetal Intestine Large intestine
11 chr1:61391600-61395400 Weak transcription Fetal Intestine Small intestine
12 chr1:61391600-61396000 Weak transcription Placenta Placenta
13 chr1:61391600-61400200 Weak transcription Fetal Brain Female brain
14 chr1:61391600-61400400 Weak transcription Fetal Brain Male brain

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