Variant report

Variant rs530478337
Chromosome Location chr6:140958497-140958498
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:140948600-140991200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:140957400-140958600 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr6:140957400-140958600 Enhancers Fetal Brain Male brain
4 chr6:140957600-140958600 Enhancers H1 Cell Line embryonic stem cell
5 chr6:140957600-140958600 Enhancers HUES48 Cell Line embryonic stem cell
6 chr6:140957600-140958600 Enhancers HUES64 Cell Line embryonic stem cell
7 chr6:140957800-140958600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr6:140958200-140958600 Enhancers Cortex derived primary cultured neurospheres brain
9 chr6:140958200-140958600 Enhancers Brain Substantia Nigra brain
10 chr6:140958200-140958800 Active TSS iPS-20b Cell Line embryonic stem cell
11 chr6:140958400-140958600 Enhancers Fetal Brain Female brain
12 chr6:140958400-140958600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
13 chr6:140958400-140958600 Enhancers Rectal Smooth Muscle rectum
14 chr6:140958400-140961800 Enhancers Fetal Heart heart

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