Variant report

Variant rs17011437
Chromosome Location chr10:50115959-50115960
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:50072800-50126200 Strong transcription Primary B cells from peripheral blood blood
2 chr10:50074600-50129600 Strong transcription Primary B cells from cord blood blood
3 chr10:50075400-50126000 Strong transcription Primary neutrophils fromperipheralblood blood
4 chr10:50101600-50122800 Weak transcription Rectal Mucosa Donor 29 rectum
5 chr10:50104800-50119200 Weak transcription Sigmoid Colon Sigmoid Colon
6 chr10:50108400-50126000 Strong transcription Primary hematopoietic stem cells short term culture blood
7 chr10:50109000-50126000 Strong transcription Monocytes-CD14+_RO01746 blood
8 chr10:50109400-50127800 Strong transcription Primary monocytes fromperipheralblood blood
9 chr10:50110200-50120400 Weak transcription Primary T cells from cord blood blood
10 chr10:50111800-50116600 Strong transcription Primary hematopoietic stem cells blood
11 chr10:50113400-50118200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr10:50113600-50118200 Weak transcription Spleen Spleen
13 chr10:50113600-50118400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr10:50114000-50120200 Weak transcription Fetal Stomach stomach
15 chr10:50114200-50116000 Enhancers Fetal Muscle Leg muscle
16 chr10:50114200-50122800 Weak transcription Lung lung
17 chr10:50114800-50117000 Weak transcription H9 Cell Line embryonic stem cell
18 chr10:50114800-50117600 Weak transcription Esophagus oesophagus
19 chr10:50115600-50116400 Genic enhancers GM12878-XiMat blood
20 chr10:50115800-50116200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
21 chr10:50115800-50116400 Strong transcription Primary mononuclear cells fromperipheralblood Blood

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