Variant report

Variant rs73668366
Chromosome Location chr9:139633207-139633208
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139623600-139635600 Weak transcription Primary T regulatory cells fromperipheralblood blood
2 chr9:139623800-139635400 Weak transcription Right Atrium heart
3 chr9:139623800-139636400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr9:139624000-139634000 Weak transcription Primary B cells from cord blood blood
5 chr9:139624000-139635200 Weak transcription Gastric stomach
6 chr9:139624000-139635600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr9:139624800-139635200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr9:139627600-139635400 Weak transcription Primary hematopoietic stem cells short term culture blood
9 chr9:139627600-139635600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr9:139628000-139633400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr9:139629600-139633400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
12 chr9:139630800-139634800 Weak transcription Fetal Thymus thymus
13 chr9:139632800-139634400 Strong transcription Primary B cells from peripheral blood blood
14 chr9:139633000-139634400 Strong transcription Right Ventricle heart
15 chr9:139633000-139635000 Strong transcription Spleen Spleen
16 chr9:139633200-139633400 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin01 Skin
17 chr9:139633200-139633400 Bivalent Enhancer Placenta Placenta
18 chr9:139633200-139633400 Enhancers K562 blood
19 chr9:139633200-139634000 Strong transcription Primary T helper naive cells fromperipheralblood blood

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