Variant report

Variant rs376316
Chromosome Location chr6:29878190-29878191
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29857200-29878400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr6:29857600-29879400 Weak transcription Stomach Smooth Muscle stomach
3 chr6:29868600-29893800 Weak transcription Aorta Aorta
4 chr6:29874400-29879200 Enhancers Fetal Intestine Large intestine
5 chr6:29875600-29878600 Enhancers Duodenum Mucosa Duodenum
6 chr6:29876400-29893800 Weak transcription Gastric stomach
7 chr6:29876600-29881600 Enhancers HepG2 liver
8 chr6:29877400-29878600 Enhancers Esophagus oesophagus
9 chr6:29877400-29878600 Enhancers GM12878-XiMat blood
10 chr6:29877400-29885600 Weak transcription Spleen Spleen
11 chr6:29877600-29878200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr6:29877600-29878400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr6:29877600-29878400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr6:29877800-29879200 Enhancers Fetal Intestine Small intestine
15 chr6:29878000-29878200 Enhancers A549 lung

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