Variant report

Variant rs17036919
Chromosome Location chr12:105687109-105687110
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:105683400-105688600 Weak transcription NHEK skin
2 chr12:105686000-105687200 Enhancers HUVEC blood vessel
3 chr12:105686200-105687200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr12:105686400-105687200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr12:105686400-105687200 Enhancers Muscle Satellite Cultured Cells --
6 chr12:105686600-105687200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr12:105686600-105687200 Enhancers Pancreatic Islets Pancreatic Islet
8 chr12:105686600-105687200 Enhancers Osteobl bone
9 chr12:105686600-105688800 Weak transcription Stomach Mucosa stomach
10 chr12:105686600-105689000 Enhancers Fetal Intestine Small intestine
11 chr12:105686800-105687200 Enhancers A549 lung
12 chr12:105686800-105687400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr12:105686800-105687400 Weak transcription Aorta Aorta
14 chr12:105686800-105687600 Weak transcription Fetal Intestine Large intestine
15 chr12:105687000-105692200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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