Variant report

Variant rs1611423
Chromosome Location chr6:29892217-29892218
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 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 chr6:29888600-29892600 Weak transcription Primary monocytes fromperipheralblood blood
9 chr6:29888600-29893200 Weak transcription Primary neutrophils fromperipheralblood blood
10 chr6:29888800-29894400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr6:29890800-29893600 Weak transcription Pancreas Pancrea
12 chr6:29891600-29893600 Enhancers HepG2 liver
13 chr6:29891800-29893400 Enhancers NHEK skin
14 chr6:29892000-29892600 Enhancers Liver Liver
15 chr6:29892000-29892800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr6:29892000-29893600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr6:29892000-29893600 Enhancers Primary T helper cells fromperipheralblood blood
18 chr6:29892000-29893600 Enhancers Fetal Intestine Small intestine
19 chr6:29892000-29893600 Enhancers HMEC breast
20 chr6:29892000-29893800 Enhancers Hela-S3 cervix
21 chr6:29892200-29893200 Enhancers Monocytes-CD14+_RO01746 blood
22 chr6:29892200-29893400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
23 chr6:29892200-29893600 Enhancers Primary T helper 17 cells PMA-I stimulated --

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