The 2.0 version of rSNPBase

Variant report

Variant rs73306148
Chromosome Location chr10:49930855-49930856
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:49922000-49933800 Weak transcription Right Atrium heart
2 chr10:49923400-49932400 Strong transcription Monocytes-CD14+_RO01746 blood
3 chr10:49923400-49960200 Strong transcription Primary hematopoietic stem cells short term culture blood
4 chr10:49923600-49939400 Weak transcription Adipose Nuclei Adipose
5 chr10:49924600-49933200 Strong transcription Primary monocytes fromperipheralblood blood
6 chr10:49925200-49951600 Strong transcription Primary B cells from peripheral blood blood
7 chr10:49926400-49953600 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr10:49927800-49949600 Strong transcription Primary mononuclear cells fromperipheralblood Blood
9 chr10:49927800-49953400 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr10:49928000-49951600 Strong transcription GM12878-XiMat blood
11 chr10:49928200-49931600 Enhancers Primary neutrophils fromperipheralblood blood
12 chr10:49928400-49953800 Strong transcription Primary hematopoietic stem cells blood
13 chr10:49929000-49931000 Enhancers HepG2 liver
14 chr10:49929200-49931000 Strong transcription Rectal Mucosa Donor 29 rectum
15 chr10:49929400-49939200 Weak transcription Lung lung
16 chr10:49930600-49932600 Genic enhancers Spleen Spleen
17 chr10:49930800-49931400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
18 chr10:49930800-49934600 Genic enhancers Primary B cells from cord blood blood

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Last update: Aug 31, 2015