Variant report

Variant rs10771467
Chromosome Location chr12:29192282-29192283
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:29190000-29194200 Weak transcription Duodenum Mucosa Duodenum
2 chr12:29191400-29192400 Enhancers NHDF-Ad bronchial
3 chr12:29191400-29194200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr12:29191400-29197200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr12:29191600-29192800 Enhancers Osteobl bone
6 chr12:29191600-29194400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr12:29191600-29196000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr12:29191800-29192400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr12:29191800-29192600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr12:29191800-29192800 Enhancers Muscle Satellite Cultured Cells --
11 chr12:29191800-29192800 Enhancers Fetal Lung lung
12 chr12:29191800-29194800 Enhancers Fetal Intestine Large intestine
13 chr12:29191800-29194800 Enhancers Fetal Intestine Small intestine
14 chr12:29191800-29197000 Enhancers NHLF lung
15 chr12:29192000-29192800 Enhancers Fetal Kidney kidney
16 chr12:29192200-29192800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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