Variant report

Variant rs17198619
Chromosome Location chr2:182190558-182190559
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:182179600-182191200 Weak transcription Primary T helper naive cells fromperipheralblood blood
2 chr2:182179800-182191000 Weak transcription Primary B cells from cord blood blood
3 chr2:182183800-182191400 Weak transcription Fetal Thymus thymus
4 chr2:182185800-182199000 Weak transcription Dnd41 blood
5 chr2:182186200-182191200 Weak transcription Primary T killer naive cells fromperipheralblood blood
6 chr2:182188400-182191200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr2:182190200-182190600 Enhancers Fetal Brain Male brain
8 chr2:182190200-182191600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
9 chr2:182190200-182192000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr2:182190400-182190800 Weak transcription Primary hematopoietic stem cells blood
11 chr2:182190400-182191600 Weak transcription iPS-20b Cell Line embryonic stem cell
12 chr2:182190400-182191800 Enhancers Primary T cells from cord blood blood

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