Variant report

Variant rs11965379
Chromosome Location chr6:30041509-30041510
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:30036800-30042400 Weak transcription Hela-S3 cervix
2 chr6:30038000-30041800 Weak transcription Ovary ovary
3 chr6:30038400-30044000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr6:30038600-30042000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:30038800-30043400 Weak transcription Dnd41 blood
6 chr6:30039000-30042000 Weak transcription Lung lung
7 chr6:30039600-30042200 Weak transcription Right Atrium heart
8 chr6:30039800-30041800 Weak transcription Gastric stomach
9 chr6:30040600-30041800 Weak transcription HMEC breast
10 chr6:30040800-30041600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr6:30041000-30041800 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
12 chr6:30041200-30041600 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
13 chr6:30041200-30041800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr6:30041200-30041800 Bivalent Enhancer Placenta Placenta
15 chr6:30041200-30042000 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
16 chr6:30041200-30042200 Enhancers Pancreas Pancrea
17 chr6:30041200-30043600 Active TSS Esophagus oesophagus
18 chr6:30041400-30041600 Enhancers NHEK skin
19 chr6:30041400-30041800 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
20 chr6:30041400-30041800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
21 chr6:30041400-30041800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
22 chr6:30041400-30041800 Bivalent Enhancer Stomach Mucosa stomach
23 chr6:30041400-30042000 Bivalent Enhancer Brain Germinal Matrix brain
24 chr6:30041400-30042200 Bivalent Enhancer Primary T helper naive cells fromperipheralblood blood
25 chr6:30041400-30043000 Flanking Bivalent TSS/Enh HepG2 liver

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