Variant report

Variant rs12278205
Chromosome Location chr11:16386755-16386756
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16379000-16387200 Weak transcription Skeletal Muscle Female skeletal muscle
2 chr11:16379200-16387400 Weak transcription Fetal Muscle Leg muscle
3 chr11:16380400-16387200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr11:16385000-16387600 Enhancers Fetal Heart heart
5 chr11:16385000-16389200 Enhancers Fetal Intestine Large intestine
6 chr11:16385000-16390200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:16385400-16388200 Enhancers Fetal Intestine Small intestine
8 chr11:16385800-16388000 Enhancers Duodenum Mucosa Duodenum
9 chr11:16386000-16387200 Enhancers Cortex derived primary cultured neurospheres brain
10 chr11:16386000-16387200 Weak transcription Small Intestine intestine
11 chr11:16386000-16387600 Weak transcription Right Atrium heart
12 chr11:16386000-16388200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr11:16386400-16387600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr11:16386400-16388000 Enhancers K562 blood
15 chr11:16386400-16388200 Enhancers Brain Germinal Matrix brain
16 chr11:16386600-16387000 Weak transcription Pancreatic Islets Pancreatic Islet
17 chr11:16386600-16387800 Enhancers Fetal Brain Female brain
18 chr11:16386600-16388000 Enhancers Brain Anterior Caudate brain
19 chr11:16386600-16389000 Enhancers Fetal Brain Male brain

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