Variant report

Variant rs3862136
Chromosome Location chr12:117551956-117551957
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:117537600-117556400 Weak transcription Right Atrium heart
2 chr12:117550000-117552600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr12:117550000-117556200 Weak transcription H1 Cell Line embryonic stem cell
4 chr12:117550400-117556000 Weak transcription Fetal Lung lung
5 chr12:117550400-117556400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr12:117550600-117558800 Weak transcription Monocytes-CD14+_RO01746 blood
7 chr12:117550800-117559200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr12:117551400-117553000 Enhancers Pancreas Pancrea
9 chr12:117551600-117552200 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr12:117551600-117566000 Weak transcription Spleen Spleen
11 chr12:117551800-117552000 Enhancers Right Ventricle heart
12 chr12:117551800-117552200 Weak transcription Fetal Thymus thymus
13 chr12:117551800-117552600 Weak transcription HepG2 liver
14 chr12:117551800-117553000 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr12:117551800-117556000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr12:117551800-117556600 Weak transcription Primary hematopoietic stem cells short term culture blood

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