Variant report

Variant rs741504
Chromosome Location chr12:31121868-31121869
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31108000-31130600 Weak transcription Fetal Brain Female brain
2 chr12:31112400-31123200 Weak transcription Lung lung
3 chr12:31112400-31126000 Weak transcription Gastric stomach
4 chr12:31113400-31123000 Weak transcription Spleen Spleen
5 chr12:31116200-31123200 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr12:31116400-31123000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr12:31116800-31122600 Strong transcription Fetal Stomach stomach
8 chr12:31117200-31128400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr12:31117400-31122800 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr12:31119000-31123400 Weak transcription Colonic Mucosa Colon
11 chr12:31119400-31123400 Weak transcription Brain Germinal Matrix brain
12 chr12:31119600-31123000 Bivalent Enhancer Fetal Muscle Leg muscle
13 chr12:31120800-31122000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
14 chr12:31120800-31125200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr12:31121000-31123400 Weak transcription Cortex derived primary cultured neurospheres brain
16 chr12:31121400-31124400 Enhancers Skeletal Muscle Male skeletal muscle
17 chr12:31121600-31122000 Weak transcription Left Ventricle heart
18 chr12:31121600-31122000 Weak transcription Right Ventricle heart
19 chr12:31121600-31123000 Weak transcription Brain Cingulate Gyrus brain
20 chr12:31121600-31123400 Weak transcription HSMMtube muscle
21 chr12:31121600-31124200 Enhancers Right Atrium heart
22 chr12:31121800-31124600 Enhancers Fetal Heart heart

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