Variant report

Variant rs11045219
Chromosome Location chr12:20553493-20553494
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:20538200-20558000 Weak transcription Left Ventricle heart
2 chr12:20542600-20566200 Weak transcription Aorta Aorta
3 chr12:20544000-20556000 Weak transcription Osteobl bone
4 chr12:20544800-20555800 Weak transcription Colon Smooth Muscle Colon
5 chr12:20548200-20556000 Weak transcription Fetal Intestine Large intestine
6 chr12:20549000-20555000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr12:20549400-20555600 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr12:20549400-20557800 Weak transcription Right Ventricle heart
9 chr12:20550400-20568200 Weak transcription Rectal Mucosa Donor 31 rectum
10 chr12:20551600-20556200 Weak transcription HUVEC blood vessel
11 chr12:20552000-20555800 Weak transcription Primary hematopoietic stem cells short term culture blood
12 chr12:20552200-20553800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr12:20552400-20553800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr12:20552400-20555600 Weak transcription Monocytes-CD14+_RO01746 blood
15 chr12:20553000-20554000 Strong transcription Hela-S3 cervix
16 chr12:20553000-20555800 Weak transcription Pancreatic Islets Pancreatic Islet
17 chr12:20553200-20554200 Strong transcription Fetal Intestine Small intestine
18 chr12:20553200-20555600 Weak transcription iPS-15b Cell Line embryonic stem cell
19 chr12:20553200-20556000 Weak transcription Fetal Heart heart
20 chr12:20553200-20571200 Weak transcription Psoas Muscle Psoas

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