Variant report

Variant rs11168718
Chromosome Location chr12:49145150-49145151
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:49134600-49161800 Weak transcription A549 lung
2 chr12:49143800-49145200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr12:49143800-49145400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr12:49144000-49145400 Enhancers Stomach Mucosa stomach
5 chr12:49144000-49147800 Weak transcription Placenta Placenta
6 chr12:49144200-49145200 Enhancers NHDF-Ad bronchial
7 chr12:49144200-49145200 Enhancers NHEK skin
8 chr12:49144200-49145400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:49144400-49145400 Enhancers Gastric stomach
10 chr12:49144600-49145200 Enhancers Primary T helper cells PMA-I stimulated --
11 chr12:49144800-49145200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr12:49144800-49158400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr12:49144800-49159400 Weak transcription HSMMtube muscle
14 chr12:49145000-49147000 Weak transcription Fetal Heart heart

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