Variant report

Variant rs10857618
Chromosome Location chr10:49900195-49900196
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:49894000-49901200 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr10:49895000-49900800 Weak transcription Primary monocytes fromperipheralblood blood
3 chr10:49895200-49904200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr10:49895200-49906200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr10:49897000-49918200 Genic enhancers Primary B cells from peripheral blood blood
6 chr10:49897400-49903200 Weak transcription Primary hematopoietic stem cells blood
7 chr10:49897800-49901600 Genic enhancers Primary B cells from cord blood blood
8 chr10:49899200-49900400 Genic enhancers Primary hematopoietic stem cells short term culture blood
9 chr10:49899600-49901200 Genic enhancers GM12878-XiMat blood
10 chr10:49899600-49903800 Weak transcription Spleen Spleen
11 chr10:49899800-49900400 Enhancers Rectal Mucosa Donor 31 rectum
12 chr10:49899800-49900800 Genic enhancers Monocytes-CD14+_RO01746 blood
13 chr10:49899800-49901000 Enhancers Primary neutrophils fromperipheralblood blood
14 chr10:49899800-49901200 Enhancers Brain Germinal Matrix brain
15 chr10:49900000-49900200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
16 chr10:49900000-49900200 Enhancers Colonic Mucosa Colon
17 chr10:49900000-49900400 Enhancers Primary Natural Killer cells fromperipheralblood blood
18 chr10:49900000-49901000 Enhancers H1 Cell Line embryonic stem cell
19 chr10:49900000-49901200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
20 chr10:49900000-49901200 Enhancers Esophagus oesophagus

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