Variant report

Variant rs573485106
Chromosome Location chr6:162622441-162622442
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162605800-162624200 Weak transcription Pancreas Pancrea
2 chr6:162620800-162623000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:162620800-162623000 Enhancers Adipose Nuclei Adipose
4 chr6:162621000-162622800 Enhancers Skeletal Muscle Female skeletal muscle
5 chr6:162621800-162623000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr6:162621800-162623000 Enhancers Fetal Heart heart
7 chr6:162622000-162622600 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr6:162622000-162623000 Enhancers Colon Smooth Muscle Colon
9 chr6:162622200-162622800 Weak transcription Skeletal Muscle Male skeletal muscle
10 chr6:162622400-162622600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr6:162622400-162622800 Enhancers Psoas Muscle Psoas
12 chr6:162622400-162624200 Weak transcription Cortex derived primary cultured neurospheres brain
13 chr6:162622400-162624400 Weak transcription Aorta Aorta
14 chr6:162622400-162624400 Weak transcription Fetal Stomach stomach
15 chr6:162622400-162632000 Weak transcription Left Ventricle heart
16 chr6:162622400-162636000 Weak transcription Right Atrium heart

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