Variant report

Variant rs61632434
Chromosome Location chr6:54775877-54775878
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:54765800-54780800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr6:54769000-54780800 Weak transcription NHEK skin
3 chr6:54770000-54781200 Weak transcription HMEC breast
4 chr6:54774600-54776600 Enhancers Fetal Lung lung
5 chr6:54774800-54781200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr6:54775000-54776000 Enhancers Fetal Intestine Large intestine
7 chr6:54775000-54776000 Enhancers Fetal Intestine Small intestine
8 chr6:54775200-54776000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr6:54775200-54776000 Enhancers Fetal Brain Male brain
10 chr6:54775600-54780800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr6:54775600-54781400 Weak transcription Duodenum Mucosa Duodenum
12 chr6:54775600-54788400 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr6:54775800-54776400 Weak transcription Pancreatic Islets Pancreatic Islet

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