Variant report

Variant rs2919699
Chromosome Location chr11:70979929-70979930
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:70977800-70980800 Weak transcription Stomach Mucosa stomach
2 chr11:70977800-70981000 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr11:70977800-70981200 Weak transcription Colonic Mucosa Colon
4 chr11:70978000-70980000 Weak transcription Rectal Mucosa Donor 31 rectum
5 chr11:70978000-70980600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:70978000-70980600 Weak transcription Placenta Amnion Placenta Amnion
7 chr11:70978000-70980800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr11:70978000-70981000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:70978600-70980600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr11:70978600-70981600 Enhancers Duodenum Mucosa Duodenum
11 chr11:70978800-70980000 Bivalent Enhancer Fetal Stomach stomach
12 chr11:70978800-70981600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr11:70979000-70980200 Enhancers Pancreas Pancrea
14 chr11:70979200-70980200 Flanking Active TSS HepG2 liver
15 chr11:70979200-70981400 Enhancers Fetal Intestine Small intestine
16 chr11:70979600-70980400 Enhancers Liver Liver
17 chr11:70979600-70980600 Weak transcription HSMM muscle
18 chr11:70979600-70980600 Weak transcription HSMMtube muscle
19 chr11:70979600-70981600 Enhancers A549 lung
20 chr11:70979800-70980000 Enhancers Fetal Brain Male brain
21 chr11:70979800-70981600 Enhancers Fetal Intestine Large intestine

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