Variant report

Variant rs9493261
Chromosome Location chr6:132592451-132592452
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132588400-132592800 Enhancers Primary B cells from cord blood blood
2 chr6:132589600-132595800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr6:132590000-132595400 Weak transcription Aorta Aorta
4 chr6:132591200-132592800 Enhancers Stomach Mucosa stomach
5 chr6:132591600-132592600 Enhancers Fetal Intestine Small intestine
6 chr6:132591800-132592600 Enhancers Fetal Intestine Large intestine
7 chr6:132591800-132592600 Enhancers Fetal Kidney kidney
8 chr6:132591800-132592600 Enhancers Fetal Muscle Leg muscle
9 chr6:132591800-132592600 Enhancers Fetal Stomach stomach
10 chr6:132591800-132592600 Enhancers Pancreas Pancrea
11 chr6:132591800-132592600 Enhancers Psoas Muscle Psoas
12 chr6:132591800-132592600 Enhancers Sigmoid Colon Sigmoid Colon
13 chr6:132592000-132592600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr6:132592000-132592600 Enhancers Duodenum Mucosa Duodenum
15 chr6:132592400-132592600 Enhancers H9 Cell Line embryonic stem cell
16 chr6:132592400-132596000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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