Variant report

Variant rs11050131
Chromosome Location chr12:29367719-29367720
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:29360400-29381000 Weak transcription HUVEC blood vessel
2 chr12:29362000-29368800 Weak transcription Primary hematopoietic stem cells blood
3 chr12:29362600-29369800 Weak transcription Primary monocytes fromperipheralblood blood
4 chr12:29363600-29369000 Weak transcription Dnd41 blood
5 chr12:29363800-29377800 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr12:29365600-29368800 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr12:29365600-29369400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr12:29365600-29370000 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr12:29365600-29370200 Weak transcription Duodenum Smooth Muscle Duodenum
10 chr12:29365600-29378600 Weak transcription Small Intestine intestine
11 chr12:29366000-29369800 Weak transcription Adipose Nuclei Adipose
12 chr12:29366000-29373800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr12:29366200-29369400 Weak transcription NHDF-Ad bronchial
14 chr12:29366200-29393200 Weak transcription Sigmoid Colon Sigmoid Colon
15 chr12:29366400-29367800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr12:29366400-29368800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr12:29366400-29369000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr12:29366400-29373800 Weak transcription Fetal Intestine Large intestine
19 chr12:29366600-29373800 Weak transcription Fetal Intestine Small intestine
20 chr12:29366800-29373600 Weak transcription Placenta Placenta
21 chr12:29367000-29368000 Enhancers Primary neutrophils fromperipheralblood blood

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