Variant report

Variant rs11890124
Chromosome Location chr2:51230894-51230895
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:51207400-51237600 Weak transcription Brain Germinal Matrix brain
2 chr2:51226000-51231200 Enhancers Pancreatic Islets Pancreatic Islet
3 chr2:51226200-51231400 Enhancers HUES64 Cell Line embryonic stem cell
4 chr2:51226200-51232200 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr2:51226800-51231200 Enhancers HUES6 Cell Line embryonic stem cell
6 chr2:51227400-51239800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr2:51228200-51238400 Weak transcription Fetal Brain Male brain
8 chr2:51228200-51238800 Weak transcription Fetal Brain Female brain
9 chr2:51228600-51234400 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr2:51229000-51232600 Weak transcription Brain Angular Gyrus brain
11 chr2:51229200-51235000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
12 chr2:51230600-51231000 Flanking Active TSS HUES48 Cell Line embryonic stem cell
13 chr2:51230600-51231200 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr2:51230600-51232000 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr2:51230600-51234000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr2:51230800-51231000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr2:51230800-51231200 Enhancers H1 Cell Line embryonic stem cell
18 chr2:51230800-51231400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
19 chr2:51230800-51231400 Enhancers Primary monocytes fromperipheralblood blood
20 chr2:51230800-51231400 Flanking Active TSS Primary neutrophils fromperipheralblood blood
21 chr2:51230800-51231400 Enhancers Brain Substantia Nigra brain
22 chr2:51230800-51231400 Enhancers HUVEC blood vessel
23 chr2:51230800-51231400 Enhancers Monocytes-CD14+_RO01746 blood
24 chr2:51230800-51231800 Enhancers H9 Cell Line embryonic stem cell

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