Variant report

Variant rs61733497
Chromosome Location chr9:139633582-139633583
allele A/G
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 chr9:139630800-139634800 Weak transcription Fetal Thymus thymus
11 chr9:139632800-139634400 Strong transcription Primary B cells from peripheral blood blood
12 chr9:139633000-139634400 Strong transcription Right Ventricle heart
13 chr9:139633000-139635000 Strong transcription Spleen Spleen
14 chr9:139633200-139634000 Strong transcription Primary T helper naive cells fromperipheralblood blood
15 chr9:139633400-139633600 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin
16 chr9:139633400-139633600 Bivalent Enhancer Duodenum Mucosa Duodenum
17 chr9:139633400-139633800 Weak transcription K562 blood
18 chr9:139633400-139634200 Strong transcription Primary mononuclear cells fromperipheralblood Blood
19 chr9:139633400-139636000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell

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