Variant report

Variant rs10801156
Chromosome Location chr1:192786384-192786385
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192779400-192790800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr1:192779600-192793200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr1:192779800-192786400 Weak transcription Small Intestine intestine
4 chr1:192781000-192795000 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr1:192781200-192791200 Weak transcription Fetal Brain Male brain
6 chr1:192781400-192786400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:192781400-192803400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr1:192781800-192795200 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr1:192782000-192794400 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr1:192784600-192790800 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr1:192785400-192786600 Enhancers Duodenum Smooth Muscle Duodenum
12 chr1:192785800-192786400 Enhancers Colon Smooth Muscle Colon
13 chr1:192785800-192786800 Enhancers Fetal Lung lung
14 chr1:192786200-192786400 Enhancers Rectal Smooth Muscle rectum
15 chr1:192786200-192786600 Flanking Active TSS Primary neutrophils fromperipheralblood blood
16 chr1:192786200-192787200 Enhancers Primary monocytes fromperipheralblood blood

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