Variant report

Variant rs9259801
Chromosome Location chr6:29892029-29892030
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29868600-29893800 Weak transcription Aorta Aorta
2 chr6:29876400-29893800 Weak transcription Gastric stomach
3 chr6:29878600-29892400 Weak transcription Duodenum Mucosa Duodenum
4 chr6:29878600-29892600 Weak transcription Esophagus oesophagus
5 chr6:29883000-29892600 Weak transcription Stomach Mucosa stomach
6 chr6:29885800-29893800 Weak transcription Spleen Spleen
7 chr6:29886600-29892600 Weak transcription Fetal Intestine Large intestine
8 chr6:29888600-29892200 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr6:29888600-29892600 Weak transcription Primary monocytes fromperipheralblood blood
10 chr6:29888600-29893200 Weak transcription Primary neutrophils fromperipheralblood blood
11 chr6:29888800-29894400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr6:29890800-29893600 Weak transcription Pancreas Pancrea
13 chr6:29891600-29893600 Enhancers HepG2 liver
14 chr6:29891800-29893400 Enhancers NHEK skin
15 chr6:29892000-29892600 Enhancers Liver Liver
16 chr6:29892000-29892800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr6:29892000-29893600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr6:29892000-29893600 Enhancers Primary T helper cells fromperipheralblood blood
19 chr6:29892000-29893600 Enhancers Fetal Intestine Small intestine
20 chr6:29892000-29893600 Enhancers HMEC breast
21 chr6:29892000-29893800 Enhancers Hela-S3 cervix

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