Variant report

Variant rs9665670
Chromosome Location chr10:26910726-26910727
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:26906000-26910800 Weak transcription Liver Liver
2 chr10:26907400-26910800 Weak transcription Fetal Thymus thymus
3 chr10:26908000-26911200 Weak transcription Right Atrium heart
4 chr10:26909400-26910800 Enhancers Fetal Intestine Small intestine
5 chr10:26909800-26910800 Weak transcription Stomach Mucosa stomach
6 chr10:26909800-26911000 Enhancers Duodenum Mucosa Duodenum
7 chr10:26910600-26910800 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
8 chr10:26910600-26910800 Enhancers Primary monocytes fromperipheralblood blood
9 chr10:26910600-26910800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr10:26910600-26910800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr10:26910600-26910800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr10:26910600-26910800 Enhancers Fetal Intestine Large intestine
13 chr10:26910600-26910800 Enhancers Rectal Mucosa Donor 31 rectum
14 chr10:26910600-26910800 Enhancers Monocytes-CD14+_RO01746 blood
15 chr10:26910600-26910800 Enhancers NHEK skin
16 chr10:26910600-26911000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr10:26910600-26911200 Enhancers Primary hematopoietic stem cells short term culture blood
18 chr10:26910600-26911800 Bivalent/Poised TSS ES-WA7 Cell Line embryonic stem cell

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